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    <title>START Center for Cancer Research Jobs</title>
    <link>https://j.brt.mv/CompanyPortal.do?companyGK=51234&amp;portalGK=41776</link>
    <description><![CDATA[Job Postings available for application.]]></description>
    <language>en-us</language>
    <pubDate>Mon, 16 Mar 2026 02:03:24 EDT</pubDate>
    <lastBuildDate>Mon, 16 Mar 2026 02:03:24 EDT</lastBuildDate>
    <generator>BrightMove ATS</generator>
    <item>
      <title><![CDATA[CTMS Entry Coordinator - Madrid, ES-M]]></title>
      <link>https://j.brt.mv/jb.do?reqGK=27773181&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>247e1347-74a8-48e3-969f-f1357c980666</guid>
      <description><![CDATA[START Center for Cancer Research (&ldquo;START&rdquo;) es la mayor red mundial de centros de fase I, dedicada por completo a la investigaci&oacute;n cl&iacute;nica oncol&oacute;gica. A lo largo de nuestra historia, START ha proporcionado esperanza a pacientes con c&aacute;ncer en consultas de comunidades globales, ofreci&eacute;ndoles acceso a ensayos de vanguardia en Estados Unidos y Europa. En la actualidad, con m&aacute;s de 1.300 estudios realizados y con centros de investigaci&oacute;n en Estados Unidos y en Espa&ntilde;a, Portugal e Irlanda, la misi&oacute;n de START es acelerar el desarrollo de nuevos medicamentos contra el c&aacute;ncer que mejoren la calidad de vida y la supervivencia de los pacientes con c&aacute;ncer y conduzcan a su eventual curaci&oacute;n. Hasta la fecha, m&aacute;s de 43 terapias realizadas en centros START han obtenido la aprobaci&oacute;n de la FDA/EMA.
Vacante disponible: CTMS Entry Coordinator
Responsabilidades:

Promover el cumplimiento de los procedimientos necesarios que pide el ensayo cl&iacute;nico 
Proteger la confidencialidad del paciente y del protocolo, aplicando los requisitos necesarios de protecci&oacute;n de datos del paciente
Colaborar con el equipo de investigaci&oacute;n para mejorar en la obtenci&oacute;n y recogida de datos de los procedimientos que se realizan al paciente desde su inclusi&oacute;n hasta su finalizaci&oacute;n en el ensayo cl&iacute;nico 
Colaborar con la Enfermera de Investigaci&oacute;n en la inclusi&oacute;n de nuevos pacientes en el CTMS, si no vuelcan correctamente desde eMR 
Obtener listado de pacientes diario desde el CTMS y eMR para incluir las visitas realizadas, retrasadas y/o apliquen, una vez se pueda revisar toda la documentaci&oacute;n
Incluir en CTMS todos los procedimientos que solicite el protocolo y que se realicen a los pacientes dentro del ensayo cl&iacute;nico, en las visitas que correspondan y ocurran 
Incluir en CTMS todos los procedimientos realizados a los pacientes dentro del ensayo cl&iacute;nico que no se soliciten por protocolo pero que se realizan de manera adicional a los pacientes dentro del ensayo
Informar a la enfermera de investigaci&oacute;n y equipo investigador de cualquier variable que encuentre entre los procedimientos realizados y los procedimientos que se esperan por calendario del protocolo 
Comunicar errores de documentos que puedan faltas, est&eacute;n incompletos o haya que enmendar en eMR al equipo investigador
Realizar formaci&oacute;n relacionada con CTMS al personal de START cuando sea necesario, para mejorar el flujo de trabajo y formar a nuevo personal 
Cumplir con los procedimientos normalizados de trabajo propios de la Unidad Fase I

Requisitos:

Inter&eacute;s y conocimiento en el &aacute;mbito sanitario
Se valorar&aacute; experiencia previa en ensayos cl&iacute;nicos
Persona proactiva y con capacidad de organizaci&oacute;n.
Excelente responsabilidad y atenci&oacute;n al detalle
Habilidad para trabajar en equipo y mantener una buena comunicaci&oacute;n con los compa&ntilde;eros y supervisores.
Nivel de ingl&eacute;s intermedio - avanzado

Beneficios

Jornada de Lunes a Viernes
29 d&iacute;as laborables de vacaciones
Retribuci&oacute;n flexible
Posibilidad de realizar clases particulares de ingl&eacute;s totalmente gratuitas
24 y 31 de diciembre libres

&iquest;Est&aacute; preparado para formar parte de un equipo que cambiar&aacute; el futuro del tratamiento del c&aacute;ncer?
&Uacute;nase a nosotros en nuestra misi&oacute;n de vencer al c&aacute;ncer, ensayo cl&iacute;nico a ensayo. Su experiencia y dedicaci&oacute;n pueden ayudarnos a llevar esperanza y curaci&oacute;n a pacientes de todo el mundo. Env&iacute;a tu solicitud en l&iacute;nea.]]></description>
      <pubDate>Mon, 09 Mar 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Scheduler - Grand Rapids, MI]]></title>
      <link>https://j.brt.mv/jb.do?reqGK=27772965&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>5661c345-daf6-450f-86e3-675eab7c9cbd</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering "Hope Through Access&rdquo; to cutting edge trials throughout the United States and Europe.  
We are seeking a Scheduler, who will facilitate excellent patient care by supporting and collaborating with the clinic team. 
Work Schedule:  8:00am-5:00pm M-F
Location:     5800 Foremost Dr SE, Grand Rapids, MI 49546
 Essential Responsibilities:

Manage scheduling protocol specific Study Schedules including, but not limited to, scheduling appointments, radiology procedures and booking hotel stays.
Ensure prior authorizations are completed.
Perform administrative responsibilities, including, but not limited to, scheduling routine follow-up and treatment appointments, managing external referrals and consults, handling no-shows, answering phone calls, and rescheduling patients.
Perform the day-to-day delivery of quality services through consistent application of policies, procedures, protocols, and standards.
Communicate with patients and visitors in a caring and respectful manner. Collaborate with other care team members and anticipate their needs to ensure coordinated patient care.
Use and maintain patient electronic medical records, including filing, faxing, and copying.
Assist with ongoing quality improvements to provide efficient, cost-effective care.
Engage in continuous education and training to maintain skills, knowledge, and competency to complete functions of role.
Other duties may be assigned at any time.

 Education & Experience:

 High School Diploma or equivalent.
One year experience in an outpatient physician practice or healthcare setting.
Effective communication skills and collaborative attitude.
Strong attention to detail.
Knowledge of medical terminology as it relates to scheduling study specific procedures such as CT/MRI/PET scans, biopsies, eye exams, etc

Preferred Education and Experience:

Oncology and/or research experience.

 Best-in-Class Benefits and Perks 
We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package&mdash;based on experience&mdash;along with comprehensive benefits designed to support you both personally and professionally:

 401(k) retirement savings plan with employer match 
Eligibility for an annual performance bonus, based on role and company results 
Generous paid time off and paid holidays 
Comprehensive medical, dental, and vision coverage and optional insurance options 
Company  paid life and disability insurance for added financial protection 
Employee Assistance Program (EAP) providing confidential, no cost support for you and your family from day one 
Flexible FSA and HSA plans to support your financial wellness 
Commitment to a supportive environment that values balance, wellbeing, and flexibility 
We&rsquo;re committed to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START, you&rsquo;ll join a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation. 

 More About START 
START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. START represents the world&rsquo;s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of &ldquo;Hope Through Access&rdquo;. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash; one of the most effective cancer drugs in medical history. 
 Learn more atSTARTresearch.com.  
 Ready to be part of a team changing the future of cancer treatment? 
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online. 
 We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Mon, 09 Mar 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Supervisor, Vivarium Operations - San Antonio, TX]]></title>
      <link>https://j.brt.mv/jb.do?reqGK=27772950&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>af3b4f0f-8204-4ddd-b3a6-507ad90023ec</guid>
      <description><![CDATA[XenoSTART, the preclinical division of START is a translational research organization focused on creating relevant preclinical cancer models.  Our xenograft models represent each cancer type and disease stage and are established from patients at our domestic and international cancer centers. The XenoSTART Patient-Derived Xenograft (XPDX) platform includes over 2,500 models annotated with each donor patient&rsquo;s cancer treatment and outcome data and characterized using IHC, DNA/RNA sequencing, and relevant in vivo drug efficacy.
Our XPDX models are clinically annotated and include patient treatment history and outcome and are characterized through genomic profiling, histologic analysis, and in vivo drug sensitivity to relevant standards of care. These models may be utilized in the following manner:

In vivo PK/PD and efficacy studies
In vivo efficacy panel screens (indication or target focused)
In licensing of models for internal studies
Custom model development
Orthotopic and radiotherapy studies
Ex vivo and organoid studies

The Supervisor, Vivarium Operations, will play a crucial role in providing an efficient and compliant vivarium. The role includes overseeing daily vivarium processes and team performance, including scheduling, training, and staff evaluation. This role involves performing PDX studies from industry-sponsored and investigator-initiated studies, ensuring adherence to protocols and compliance with all regulatory and safety guidelines, training and scheduling all procedures related to small animal handling, husbandry, surgery, sterile environments, and dosing. This position will also support the optimization of standard operating procedures and working instructions to ensure quality and effectiveness.
 
Essential Responsibilities

Support the Manager, Vivarium in overseeing daily vivarium operations, including supervision of research associates: hiring, onboarding, training, work assignments, time off approval, payroll, performance evaluations, employee development plans, and performance improvement.
Provide training and hands-on study support on technical procedures, including animal handling, dosing, surgery, tumor implantation, euthanasia, sample collection/processing and data entry.
Schedule daily tasks, including resolving conflicts and coordinating efforts across multiple teams.
Create and revise SOPs, working instructions, and other laboratory documentation.
Monitor animal health and maintain accurate records of experiments and results in compliance with institutional and regulatory guidelines.
Ensure the health and welfare of animals to maintain compliance with Association for Assessment and Accreditation of Laboratory Animal Care, International (AAALAC) and Institutional Animal Care and Use Committee (IACUC) standards.
Confirm all study-related documentation is current, accurate, and audit-ready.
Identify and escalate quality or compliance concerns to the appropriate supervisor or project manager.

Education & Experience

Bachelor&rsquo;s degree in animal care or science field.
2-4 years of supervisory experience in an animal facility.
Formal training in animal handling and in vivo research procedures.
Experience with animal handling, dosing, and necropsy procedures.
Familiarity with regulatory requirements and ethical standards for animal research.
Strong communication skills and ability to effectively communicate and present summaries of research results to team members.
Strong organizational skills with great attention to details and ability to troubleshoot problems.

Preferred Education and Experience:

Supervisory experience in a preclinical research setting.
Familiarity with Association for Assessment and Accreditation of Laboratory Animal Care, International (AAALAC), Institutional Animal Care and Use Committee (IACUC), and OSHA compliance.

Physical and Travel Requirements: 

Ability to stand for extended periods of time.
Ability to perform daily tasks requires fine motor skills.
Ability to utilize full range of motion (reaching, bending, etc.).
Ability to lift 40 pounds.
Ability to handle and understand safety procedures associated with biological, investigational, or hazardous materials, not to exceed Biosafety Level 2 (BSL2).
Ability to work with and understand safety procedures associated with Sharps Disposal Containers, including but not limited to needles, scalpel blades, lancets, etc.
Ability to don full Personal Protective Equipment (PPE) on shift, including but not limited to lab coat, gloves, mask, and bouffant.

Best-in-Class Benefits and Perks

We value our employees&rsquo; time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:
Comprehensive health coverage: Medical, dental, and vision insurance provided
Robust retirement planning: 401(k) plan available with employer matching
Financial security: Life and disability insurance for added protection
Flexible financial options: Health savings and flexible spending accounts offered
Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided
Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.

More about The START Center for Cancer Research
Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including for 43 therapies that were approved by the FDA. START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. Learn more at STARTresearch.com.
Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.
We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Mon, 09 Mar 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Auxiliar Documentalista (Contrato Temporal) - Madrid, ES-M]]></title>
      <link>https://j.brt.mv/jb.do?reqGK=27772930&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>f3b73838-4d68-48c2-b8d5-c0cb5907c522</guid>
      <description><![CDATA[START Center for Cancer Research (&ldquo;START&rdquo;) es la mayor red mundial de centros de fase I, dedicada por completo a la investigaci&oacute;n cl&iacute;nica oncol&oacute;gica. A lo largo de nuestra historia, START ha proporcionado esperanza a pacientes con c&aacute;ncer en consultas de comunidades globales, ofreci&eacute;ndoles acceso a ensayos de vanguardia en Estados Unidos y Europa. En la actualidad, con m&aacute;s de 1.300 estudios realizados y con centros de investigaci&oacute;n en Estados Unidos y en Espa&ntilde;a, Portugal e Irlanda, la misi&oacute;n de START es acelerar el desarrollo de nuevos medicamentos contra el c&aacute;ncer que mejoren la calidad de vida y la supervivencia de los pacientes con c&aacute;ncer y conduzcan a su eventual curaci&oacute;n. Hasta la fecha, m&aacute;s de 43 terapias realizadas en centros START han obtenido la aprobaci&oacute;n de la FDA/EMA.
Vacante disponible: Auxiliar Documentalista - Ensayos Cl&iacute;nicos Oncol&oacute;gicos (Contrato Temporal)
Responsabilidades:

Preparar la documentaci&oacute;n para las firmas requeridas el d&iacute;a de la visita de inicio 
Revisar la documentaci&oacute;n del investigador de cara a visitas de cierre o auditar&iacute;as
Recepcionar la documentaci&oacute;n de los ensayos cl&iacute;nicos abiertos en la Unidad
Actualizar informaci&oacute;n en las plataformas que apliquen 
Mantener la confidencialidad de la documentaci&oacute;n del ensayo cl&iacute;nico
Gestionar la obtenci&oacute;n de las firmas electr&oacute;nicas de los trainings y de los ensayos abiertos

Requisitos:

Inter&eacute;s en el &aacute;mbito sanitario
Se valorar&aacute; experiencia previa en ensayos cl&iacute;nicos
Persona proactiva y con capacidad de organizaci&oacute;n.
Excelente responsabilidad y atenci&oacute;n al detalle
Habilidad para trabajar en equipo y mantener una buena comunicaci&oacute;n con los compa&ntilde;eros y supervisores.
Nivel de ingl&eacute;s intermedio 

Beneficios

Jornada de Lunes a Viernes
29 d&iacute;as laborables de vacaciones
Retribuci&oacute;n flexible
Posibilidad de realizar clases particulares de ingl&eacute;s totalmente gratuitas
24 y 31 de diciembre libres

&iquest;Est&aacute; preparado para formar parte de un equipo que cambiar&aacute; el futuro del tratamiento del c&aacute;ncer?
&Uacute;nase a nosotros en nuestra misi&oacute;n de vencer al c&aacute;ncer, ensayo cl&iacute;nico a ensayo. Su experiencia y dedicaci&oacute;n pueden ayudarnos a llevar esperanza y curaci&oacute;n a pacientes de todo el mundo. Env&iacute;a tu solicitud en l&iacute;nea.]]></description>
      <pubDate>Sun, 08 Mar 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Clinic Nurse - West Valley City, UT]]></title>
      <link>https://j.brt.mv/jb.do?reqGK=27772716&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>86f81011-3098-4597-ac77-6575eb0bad18</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering "Hope Through Access&rdquo; to cutting edge trials throughout the United States and Europe.  
 We are seeking a Clinic Nurse. The Clinic Nurse is responsible for assisting the clinic providers with examination, evaluation and triage of individuals who are participants in research protocols that are conducted at START. The Clinic Nurse uses appropriate professional judgment and decision-making in planning and providing care. Nursing care is to be delivered in a manner consistent with the Standard Operating Procedures and standards of practice, and professional evidence-based standards
Location: West Valley, UT
Essential Responsibilities:
Patient Care

Perform telephone triage assessments of patients on trial when necessary. 
Provide patient education regarding participation in a clinical trial, chemotherapy/immunotherapy/investigational agent administration and potential side eects. 
Enter patient history into the Electronic Medical Record based on records received and the patient provided history. 
Perform basic patient assessment including physical exam, vital signs, ECG&rsquo;s and other patient assessments as needed. 
Use nursing assessment skills to observe participant&rsquo;s general well-being. Document and take appropriate action as needed. 
Provide patients with visit summaries. 
Ensure that the dignity, health, safety, and welfare of participants are given the highest priority at all times. 
Coordinate patient care with internal and external sta. 
Respond to emergency situations based upon nursing standards.
Provide coverage for Infusion Nurse as directed by management. 

Planning and problem-solving tasks 

Prepare for clinic day ensuring necessary supplies/results are available. 
Assist with prescription rells. 
Assist with entry and completion of quality standards for EHR/PQRS. 

Communicating tasks 

Provide telephone triage. 
Assist with the training and mentorship of less tenured sta. 
Complete preauthorization forms for medications and procedures. 
Assist in the referral process to specialists. 
Communicate and interact with peers and other departments in a manner that is viewed as having a positive eect on patient services and sta morale. Interact eectively with patients/family members and demonstrate sensitivity in regards to cultural diversity, age specic needs and condentiality. 

Protocol management tasks 

Work with the physician to ensure that necessary labs and assessments are performed and results are obtained. 
Work with the physician to ensure that orders are completed.  

Technical and quality tasks 

Working knowledge of a variety of health care equipment. 
Serve as a team member by expanding his/her responsibilities as directed by management to facilitate optimal workow within the cancer center. 
Time management and organizational skills.
Eective written and verbal communication skills. 

Education & Experience

High School Diploma or GED. 
Licensed Registered Nurse in practicing state.  
1-year oncology experience. 
Basic Life Support (BLS) Certification, an AHA (American Heart Association) certificate.
Experience working with Microsoft Office, including Teams, Excel, Outlook and Word.   

Preferred Experience

Bachelor&rsquo;s degree of Nursing.  
Oncology Certified Nurse (OCN). 
ONS/ONCC Chemotherapy Immunotherapy Certificate&trade; completed within the last 5 years or obtained within first year of employment.   
Clinical Trials experience. 

Best-in-Class Benefits and Perks 
We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package&mdash;based on experience&mdash;along with comprehensive benefits designed to support you both personally and professionally:  

401(k) retirement savings plan with employer match 
Eligibility for an annual performance bonus, based on role and company results 
Generous paid time off and paid holidays 
Comprehensive medical, dental, and vision coverage and optional insurance options 
Companypaid life and disability insurance for added financial protection 
Employee Assistance Program (EAP) providing confidential, nocost support for you and your family from day one 
Flexible FSA and HSA plans to support your financial wellness 
Commitment to a supportive environment that values balance, wellbeing, and flexibility 
We&rsquo;re committed to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START, you&rsquo;ll join a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation. 

More About START 
START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. START represents the world&rsquo;s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of &ldquo;Hope Through Access&rdquo;. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash; one of the most effective cancer drugs in medical history. 
 Learn more atSTARTresearch.com.  
 Ready to be part of a team changing the future of cancer treatment? 
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online. 
 We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Wed, 04 Mar 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Infusion Nurse - Lake Success, NY]]></title>
      <link>https://j.brt.mv/jb.do?reqGK=27772712&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>2d811b0c-d2be-4f19-90cc-5cad86a6a9e3</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largestearly phasesite network, fully dedicated tooncologyclinical research.Throughout ourhistory, START has provided hope to cancer patients inglobalcommunity practices by offering"Hope Through Access&rdquo;tocutting edgetrials throughout the UnitedStatesand Europe. 
 
We are hiring an Infusion Nurse who will be responsible for providing direct patient care to individuals who are participants in research protocols that are conducted at START. The Infusion Nurse uses appropriate professional judgment and decision-making in planning and providing care. Nursing care is to be delivered in a manner consistent with the Standard Operating Procedures and standards of practice, and professional evidence-based standards.
This position is offered at a pay range of $55.00 to $65.00 per hour, based on experience, qualifications, and internal equity. In addition, employees in this role may be eligible for an annual bonus of up to 10% of base earnings.
Work Schedule: 8:00 am-5:00 pm EST, Monday-Friday 
Location: 405 Lakeville Road, Entrance A, Lake Success, NY 11042
Essential Responsibilities
Patient Care

Administer chemotherapy/immunotherapy/investigational agent to participants (inclusive of parenteral) according to the protocol and applicable regulations.
Perform study-related activities including but not limited to venipuncture, obtaining blood specimens, IV insertion, and venous access device (central line) management, ECG collection, and vital signs.
Collect biological samples according to the protocol and Standard Operating Procedures.
Educate, explain, and inform participants of study procedures.
Record data obtained according to the protocol and Standard Operating Procedures.
Use nursing assessment skills to observe participant general well-being and potential adverse events. Document events and take appropriate action as needed.
Respond to emergency situations based upon nursing standards.
Provide patient education regarding participation in a clinical trial, chemotherapy/immunotherapy/investigational agent administration and potential side effects.
Ensure that the dignity, health, safety, and welfare of participants are given the highest priority at all times.

Planning and problem-solving tasks

Prepare for clinic day ensuring necessary supplies.
Assist with entry and completion of quality standards for EHR/PQRS.

Communicating tasks

Assist with the training and mentorship of less tenured staff.
Communicate with providers regarding a change in patient status.
Communicate and interact with peers and other departments in a manner that is viewed as having a positive eect on patient services and sta morale. Interact eectively with patients/family members and demonstrate sensitivity in regard to cultural diversity, age specic needs and condentiality.

Protocol Management tasks

Work with study team to ensure that study related procedures, drug administration, labs, vital signs and ECG are completed. 

Technical and Quality Tasks

Use skills, knowledge, nursing diagnosis, and clinical judgement in order to provide a high standard of care for participants in clinical trials.
Remain current with appropriate emergency certifications and company emergency policy and procedures.
Able to work effectively and efficiently under tight deadlines, high volumes and multiple interruptions.
Other duties may be assigned at any time.


Education & Experience

High School Diploma or GED.
Licensed Registered Nurse in practicing state.
Basic Life Support (BLS) certification, and AHA certified program. 
Previous experience in peripheral IV insertion and management of venous access device(s).   


Preferred Education and Experience:

1 year of experience.
Oncology Certified Nurse (OCN).
Clinical Trial and oncology experience.
Experience working with Microsoft Office, including Teams, Excel and Word. 
Advanced Cardiac Life Support (ACLS) Certification, an AHA certified program.  Can be obtained within 90 days of hire. 
ONS/ONCC Chemotherapy Immunotherapy Certificate&trade;.  Can be obtained within first year of employment.

Physical & Travel Requirements:

80% of time spent standing and/or walking.
Ability to lift up to a 60-pound weight load.
Very frequent lifting and bending, pushing and/or pulling loads.
Able to perform manual tasks that require the use of ne muscle motor skills.


Best-in-Class Benefits and Perks
We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package&mdash;based on experience&mdash;along with comprehensive benefits designed to support you both personally and professionally: 
Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.




401(k) retirement savings plan with employer match 






Eligibility for an annual performance bonus, based on role and company results 






Generous paid time off and paid holidays 






Comprehensive medical, dental, and vision coverageand optional insuranceoptions 






Company paid life and disability insurance for added financial protection 






Employee Assistance Program (EAP) providing confidential, no cost support for you and your family from day one 








Flexible FSA and HSA plans to support your financial wellness 






Commitment to a supportive environment that values balance, wellbeing, and flexibility 






We&rsquo;recommitted to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START,you&rsquo;lljoin a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation. 





More about The START Center for Cancer Research
START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. STARTrepresentsthe world&rsquo;s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of &ldquo;Hope Through Access&rdquo;.As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash;one ofthe most effective cancerdrugsin medical history. Learn more atSTARTresearch.com. 

Ready to be part of a team changing the future of cancer treatment? 
Join us in our mission to conquer cancer, one clinical trial at a time. Yourexpertiseand dedication can help us bring hope and healing to patients worldwide.Pleasesubmityour application online. 

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Wed, 04 Mar 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Infusion Nurse - GRAND RAPIDS, MI]]></title>
      <link>https://j.brt.mv/jb.do?reqGK=27772698&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>9dbc60dd-2c3b-45e9-bdc7-25f1846d477b</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largestearly phasesite network, fully dedicated tooncologyclinical research.Throughout ourhistory, START has provided hope to cancer patients inglobalcommunity practices by offering"Hope Through Access&rdquo;tocutting edgetrials throughout the UnitedStatesand Europe. 
 
We are hiring an Infusion Nurse who will be responsible for providing direct patient care to individuals who are participants in research protocols that are conducted at START. The Infusion Nurse uses appropriate professional judgment and decision-making in planning and providing care. Nursing care is to be delivered in a manner consistent with the Standard Operating Procedures and standards of practice, and professional evidence-based standards.
This position is offered at a pay range of $35.00 to $40.00 per hour, based on experience, qualifications, and internal equity. In addition, employees in this role may be eligible for an annual bonus of up to 10% of base earnings.
Work Schedule: 7:30 am-6:00 pm EST (4 days a week)
Location: 5800 Foremost Dr. SE, Grand Rapids, MI 49546
Essential Responsibilities
Patient Care

Administer chemotherapy/immunotherapy/investigational agent to participants (inclusive of parenteral) according to the protocol and applicable regulations.
Perform study-related activities including but not limited to venipuncture, obtaining blood specimens, IV insertion, and venous access device (central line) management, ECG collection, and vital signs.
Collect biological samples according to the protocol and Standard Operating Procedures.
Educate, explain, and inform participants of study procedures.
Record data obtained according to the protocol and Standard Operating Procedures.
Use nursing assessment skills to observe participant general well-being and potential adverse events. Document events and take appropriate action as needed.
Respond to emergency situations based upon nursing standards.
Provide patient education regarding participation in a clinical trial, chemotherapy/immunotherapy/investigational agent administration and potential side effects.
Ensure that the dignity, health, safety, and welfare of participants are given the highest priority at all times.

Planning and problem-solving tasks

Prepare for clinic day ensuring necessary supplies.
Assist with entry and completion of quality standards for EHR/PQRS.

Communicating tasks

Assist with the training and mentorship of less tenured staff.
Communicate with providers regarding a change in patient status.
Communicate and interact with peers and other departments in a manner that is viewed as having a positive eect on patient services and sta morale. Interact eectively with patients/family members and demonstrate sensitivity in regard to cultural diversity, age specic needs and condentiality.

Protocol Management tasks

Work with study team to ensure that study related procedures, drug administration, labs, vital signs and ECG are completed. 

Technical and Quality Tasks

Use skills, knowledge, nursing diagnosis, and clinical judgement in order to provide a high standard of care for participants in clinical trials.
Remain current with appropriate emergency certifications and company emergency policy and procedures.
Able to work effectively and efficiently under tight deadlines, high volumes and multiple interruptions.
Other duties may be assigned at any time.


Education & Experience

High School Diploma or GED.
Licensed Registered Nurse in practicing state.
Basic Life Support (BLS) certification, and AHA certified program. 
Previous experience in peripheral IV insertion and management of venous access device(s).   


Preferred Education and Experience:

1 year of experience.
Oncology Certified Nurse (OCN).
Clinical Trial and oncology experience.
Experience working with Microsoft Office, including Teams, Excel and Word. 
Advanced Cardiac Life Support (ACLS) Certification, an AHA certified program.  Can be obtained within 90 days of hire. 
ONS/ONCC Chemotherapy Immunotherapy Certificate&trade;.  Can be obtained within first year of employment.

Physical & Travel Requirements:

80% of time spent standing and/or walking.
Ability to lift up to a 60-pound weight load.
Very frequent lifting and bending, pushing and/or pulling loads.
Able to perform manual tasks that require the use of ne muscle motor skills.


Best-in-Class Benefits and Perks
We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package&mdash;based on experience&mdash;along with comprehensive benefits designed to support you both personally and professionally: 
Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.




401(k) retirement savings plan with employer match 






Eligibility for an annual performance bonus, based on role and company results 






Generous paid time off and paid holidays 






Comprehensive medical, dental, and vision coverageand optional insuranceoptions 






Company paid life and disability insurance for added financial protection 






Employee Assistance Program (EAP) providing confidential, no cost support for you and your family from day one 








Flexible FSA and HSA plans to support your financial wellness 






Commitment to a supportive environment that values balance, wellbeing, and flexibility 






We&rsquo;recommitted to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START,you&rsquo;lljoin a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation. 





More about The START Center for Cancer Research
START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. STARTrepresentsthe world&rsquo;s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of &ldquo;Hope Through Access&rdquo;.As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash;one ofthe most effective cancerdrugsin medical history. Learn more atSTARTresearch.com. 

Ready to be part of a team changing the future of cancer treatment? 
Join us in our mission to conquer cancer, one clinical trial at a time. Yourexpertiseand dedication can help us bring hope and healing to patients worldwide.Pleasesubmityour application online. 

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Wed, 04 Mar 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Clinic Nurse - FORT WORTH, TX]]></title>
      <link>https://j.brt.mv/jb.do?reqGK=27772694&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>c702c8a2-cf4f-4872-884d-8b5cf7ac3832</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering "Hope Through Access&rdquo; to cutting edge trials throughout the United States and Europe.  
 We are seeking a Clinic Nurse. The Clinic Nurse is responsible for assisting the clinic providers with examination, evaluation and triage of individuals who are participants in research protocols that are conducted at START. The Clinic Nurse uses appropriate professional judgment and decision-making in planning and providing care. Nursing care is to be delivered in a manner consistent with the Standard Operating Procedures and standards of practice, and professional evidence-based standards
Work Schedule: Monday-Friday, 8am-5pm
Location: Fort Worth, TX
Essential Responsibilities:
Patient Care

Perform telephone triage assessments of patients on trial when necessary. 
Provide patient education regarding participation in a clinical trial, chemotherapy/immunotherapy/investigational agent administration and potential side eects. 
Enter patient history into the Electronic Medical Record based on records received and the patient provided history. 
Perform basic patient assessment including physical exam, vital signs, ECG&rsquo;s and other patient assessments as needed. 
Use nursing assessment skills to observe participant&rsquo;s general well-being. Document and take appropriate action as needed. 
Provide patients with visit summaries. 
Ensure that the dignity, health, safety, and welfare of participants are given the highest priority at all times. 
Coordinate patient care with internal and external sta. 
Respond to emergency situations based upon nursing standards. 


Provide coverage for Infusion Nurse as directed by management. 

Planning and problem-solving tasks 

Prepare for clinic day ensuring necessary supplies/results are available. 
Assist with prescription rells. 
Assist with entry and completion of quality standards for EHR/PQRS. 

Communicating tasks 

Provide telephone triage. 
Assist with the training and mentorship of less tenured sta. 
Complete preauthorization forms for medications and procedures. 
Assist in the referral process to specialists. 
Communicate and interact with peers and other departments in a manner that is viewed as having a positive eect on patient services and sta morale. Interact eectively with patients/family members and demonstrate sensitivity in regards to cultural diversity, age specic needs and condentiality. 

Protocol management tasks 

Work with the physician to ensure that necessary labs and assessments are performed and results are obtained. 
Work with the physician to ensure that orders are completed.  

Technical and quality tasks 

Working knowledge of a variety of health care equipment. 
Serve as a team member by expanding his/her responsibilities as directed by management to facilitate optimal workow within the cancer center. 
Time management and organizational skills.
Eective written and verbal communication skills. 

Education & Experience

High School Diploma or GED. 
Licensed Registered Nurse in practicing state.  
1-year oncology experience. 
Basic Life Support (BLS) Certification, an AHA (American Heart Association) certificate.
Experience working with Microsoft Office, including Teams, Excel, Outlook and Word.   

Preferred Experience

Bachelor&rsquo;s degree of Nursing.  
Oncology Certified Nurse (OCN). 
ONS/ONCC Chemotherapy Immunotherapy Certificate&trade; completed within the last 5 years or obtained within first year of employment.   
Clinical Trials experience. 

Best-in-Class Benefits and Perks 
We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package&mdash;based on experience&mdash;along with comprehensive benefits designed to support you both personally and professionally:  

401(k) retirement savings plan with employer match 
Eligibility for an annual performance bonus, based on role and company results 
Generous paid time off and paid holidays 
Comprehensive medical, dental, and vision coverage and optional insurance options 
Companypaid life and disability insurance for added financial protection 
Employee Assistance Program (EAP) providing confidential, nocost support for you and your family from day one 
Flexible FSA and HSA plans to support your financial wellness 
Commitment to a supportive environment that values balance, wellbeing, and flexibility 
We&rsquo;re committed to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START, you&rsquo;ll join a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation. 

More About START 
START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. START represents the world&rsquo;s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of &ldquo;Hope Through Access&rdquo;. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash; one of the most effective cancer drugs in medical history. 
 Learn more atSTARTresearch.com.  
 Ready to be part of a team changing the future of cancer treatment? 
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online. 
 We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Wed, 04 Mar 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Administrative Research Assistant - Myrtle Beach, SC]]></title>
      <link>https://j.brt.mv/jb.do?reqGK=27772726&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>60fd7f65-1675-4be4-8bff-d871ec215d61</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering "Hope Through Access&rdquo; to cutting edge trials throughout the United States and Europe.  
 We are seeking an Administrative Research Assistant.  This role will assist the Clinical Research Coordinators in all tasks to support their roles. It will require an understanding of research terminology and basic protocol interpretation. 
Work Schedule: Monday-Friday, 8am-5pm
Location: Myrtle Beach, SC
 Essential Responsibilities

Collect, de-identify, enter/transcribe, and transmit/submit clinical data in paper and/or electronic case reports forms (CRFs), including correction and query resolution for assigned investigational drug studies. This includes but is not limited to images, lab results, and ECGs.  
Collaborate with Clinical Research Coordinator to ensure data timepoints are accurate and provide query resolution.
Contact patients in follow-up as needed per protocol.
Review and utilize protocols as guides for study activities for assigned studies.
Assist with the setup and formatting of study-specific Eligibility, Study Schedules, and Flow Sheets documents per protocol.
Assist with CTMS upkeep, including but not limited to tracking patient visits, IRB re-consents, Serious Adverse Events (SAEs) and Deviations.
Ensure that data transmissions remain current for assigned studies.
Provide support and information to onsite and remote monitors as necessary.
Comply with all applicable regulations, guidelines, and procedures pertaining to data loading, EDC systems, and clinical research.
Share responsibility with Data Coordinators to identify lab facilities and normal lab values used for assigned studies so that lab certifications can be requested for the study file.
Attend meetings regarding assigned studies as needed, including site initiation visits, Roster meetings and Forms Committee.
Communicate as needed with accounts receivable staff regarding transmitted data.
Other duties may be assigned at any time.

 
 Required Education and Experience:

High School diploma or equivalent.
One year of research administrative experience within a healthcare, pharmaceutical, or research organization.
Knowledge and training in general office administration skills, including computer applications, filing systems, etc.  
Familiarity with medical terminology.
Strong organizational skills and a sense of timeliness in completing projects.
Must be detail-oriented and able to understand instructions and work independently. 

 Best-in-Class Benefits and Perks 
We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package&mdash;based on experience&mdash;along with comprehensive benefits designed to support you both personally and professionally:   

401(k) retirement savings plan with employer match 
Eligibility for an annual performance bonus, based on role and company results 
Generous paid time off and paid holidays 
Comprehensive medical, dental, and vision coverage and optional insurance options 
Companypaid life and disability insurance for added financial protection 
Employee Assistance Program (EAP) providing confidential, nocost support for you and your family from day one 
Flexible FSA and HSA plans to support your financial wellness 
Commitment to a supportive environment that values balance, wellbeing, and flexibility 
We&rsquo;re committed to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START, you&rsquo;ll join a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation. 

 More About START 
START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. START represents the world&rsquo;s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of &ldquo;Hope Through Access&rdquo;. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash; one of the most effective cancer drugs in medical history. 
 Learn more atSTARTresearch.com.  
 Ready to be part of a team changing the future of cancer treatment? 
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online. 
 We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Wed, 04 Mar 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Lead, Regulatory Operations (Remote) - Grand Rapids, MI]]></title>
      <link>https://j.brt.mv/jb.do?reqGK=27772663&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>77a8c9a4-88c5-41e1-8f2a-240bc6345b0a</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largestearly phasesite network, fully dedicated tooncologyclinical research.Throughout ourhistory, START has provided hope to cancer patients inglobalcommunity practices by offering"Hope Through Access&rdquo;tocutting edgetrials throughout the UnitedStatesand Europe. 
We areseekingaLead, Regulatory Operations (Remote) who will serve as the regulatory subject-matter expert (SME) and provides guidance, training, and operational oversight to the Regulatory Operations team. This role oversees complex regulatory submissions, supports process improvement initiatives, delegates and prioritizes work as needed, performs quality reviews to ensure compliance and accuracy.  The Lead will prepare and submit regulatory documents for new and ongoing clinical studies to the Institutional Review Board (IRB), US Food and Drug Administration (FDA), and Institutional Biosafety Committee (IBC). This role requires strong problemsolving ability, sound judgment, and a high degree of independence.  As team lead, ensure turnaround times are met, collect and review key metrics and continually improve processes to help achieve goals. 
This is a remote role. The annual base salary for this role is $80,000 - $105,000. However, base pay may vary depending on multiple individualized factors including market location, job-related knowledge, skills, and experience. A 10% annual performance bonus is offered as well.
Essential Responsibilities: 

Ensure turnaround times are met and actively seek ways to enhances processes to ensure departmental goals are consistently achieved.  
Prepare and submit new study applications and amendments to the IRB, including drafting and negotiating informed consent forms (ICFs) with Sponsors/CROs. 
Serve as the primary point of contact for assigned studies with the IRB, IBC, and FDA. 
Prepare and submit regulatory documents including revised protocols, investigator brochures, safety reports, deviations, clarifications, continuing review reports, and closure documents. 
Prepare and submit Expanded Access and other complex or highrisk study submissions to the FDA. 
Track all submissions in FileMaker or applicable systems and maintain accurate status updates. 
Maintain complete, accurate, and auditready Investigator Site Files (ISF), both paper and electronic. 
Lead and manage regulatory closeout responsibilities for assigned studies. 
Train, mentor, and support Regulatory Operations team members, ensuring accurate submissions and proper regulatory filing. 
Perform quality control (QC) reviews of submissions and regulatory documents prepared by staff. 
Assist in work prioritization, workflow management, and crossfunctional coordination. 
Serve as the escalation point for complex regulatory questions or study challenges. 
Attend and represent Regulatory Operations in weekly Phase I meetings, Protocol Review, and Site Initiation Visits. 
Collaborate with other departments to resolve regulatory issues and ensure timely submission of deliverables. 
Develop, revise, and implement Work Instructions and SOPs. 
Assist with regulatory file preparation for audits and inspections; participate in CAPA development. 
Partner with leadership to improve regulatory processes, systems, and standardization across START USA sites. 

Education & Experience: 

Bachelor&rsquo;s degree or equivalent experience.   
Minimum 5&ndash;7 years of regulatory experience in clinical research, including new study submissions 
Advanced knowledge of IRB, IBC, and FDA submission requirements. 
Proficiency with Microsoft Word and FileMaker Pro (or similar regulatory tracking systems). 
Exceptional organizational skills with attention to detail, accuracy, and completeness. 
Ability to independently manage multiple priorities, deadlines, and complex tasks. 

Best-in-Class Benefits and Perks 
We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package&mdash;based on experience&mdash;along with comprehensive benefits designed to support you both personally and professionally: 

401(k) retirement savings plan with employer match 
Eligibility for an annual performance bonus, based on role and company results 
Generous paid time off and paid holidays 
Comprehensive medical, dental, and vision coverageand optional insuranceoptions 
Company paid life and disability insurance for added financial protection 
Employee Assistance Program (EAP) providing confidential, no cost support for you and your family from day one 
Flexible FSA and HSA plans to support your financial wellness 
Commitment to a supportive environment that values balance, wellbeing, and flexibility 
We&rsquo;recommitted to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START,you&rsquo;lljoin a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation. 

More About START 
START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. STARTrepresentsthe world&rsquo;s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of &ldquo;Hope Through Access&rdquo;.As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash;one ofthe most effective cancerdrugsin medical history. 
Learn more atSTARTresearch.com. 
Ready to be part of a team changing the future of cancer treatment? 
Join us in our mission to conquer cancer, one clinical trial at a time. Yourexpertiseand dedication can help us bring hope and healing to patients worldwide.Pleasesubmityour application online. 
We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Wed, 04 Mar 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Farmacéutico - Oncología - Madrid, ES-M]]></title>
      <link>https://j.brt.mv/jb.do?reqGK=27772688&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>ff62b791-cb78-4df6-8ca4-dc75a2396790</guid>
      <description><![CDATA[START Center for Cancer Research (&ldquo;START&rdquo;) es la mayor red mundial de centros de fase I, dedicada por completo a la investigaci&oacute;n cl&iacute;nica oncol&oacute;gica. A lo largo de nuestra historia, START ha proporcionado esperanza a pacientes con c&aacute;ncer en consultas de comunidades globales, ofreci&eacute;ndoles acceso a ensayos de vanguardia en Estados Unidos y Europa. En la actualidad, con m&aacute;s de 1.300 estudios realizados y con centros de investigaci&oacute;n en Estados Unidos y en Espa&ntilde;a, Portugal e Irlanda, la misi&oacute;n de START es acelerar el desarrollo de nuevos medicamentos contra el c&aacute;ncer que mejoren la calidad de vida y la supervivencia de los pacientes con c&aacute;ncer y conduzcan a su eventual curaci&oacute;n. Hasta la fecha, m&aacute;s de 43 terapias realizadas en centros START han obtenido la aprobaci&oacute;n de la FDA/EMA.
Vacante disponible: Farmac&eacute;utico - Ensayos Cl&iacute;nicos Oncol&oacute;gicos
Responsabilidades:

 Validaci&oacute;n de tratamientos Onco-Hematol&oacute;gicos
Revisi&oacute;n y registro de interacciones de la medicaci&oacute;n con los f&aacute;rmacos de investigaci&oacute;n, en el screening y durante el tratamiento. 
Revisi&oacute;n de adherencia a los tratamientos de administraci&oacute;n oral 
Realizaci&oacute;n de documentaci&oacute;n espec&iacute;fica por ensayo.
Gesti&oacute;n y control de los medicamentos en investigaci&oacute;n/material fungible usado en los ensayos
Gesti&oacute;n de las visita de monitores
Asesoramiento farmac&eacute;utico a los investigadores, a Enfermer&iacute;a de Investigaci&oacute;n y de tratamiento y a data managers.
Asesoramiento al promotor/monitor de los sistemas de administraci&oacute;n, material de preparaci&oacute;n y sueros disponibles. 
Asistencia a las reuniones semanales con el equipo. 

Cualificaciones y aptitudes

Licenciatura en Farmacia 
Especialidad v&iacute;a FIR en Farmacia Hospitalaria
Valorable experiencia previa en validaci&oacute;n de tratamientos Onco-Hematol&oacute;gicos y ensayos cl&iacute;nicos.
Adecuado manejo de ingl&eacute;s (hablado y escrito)
Debe ser capaz de trabajar bien en un entorno de ritmo r&aacute;pido y ser muy organizado
Excelentes dotes de comunicaci&oacute;n

Beneficios

Jornada de Lunes a Viernes (Festivos y Fines de Semana libres)
30 d&iacute;as laborables de vacaciones
Retribuci&oacute;n flexible
Posibilidad de realizar clases particulares de ingl&eacute;s totalmente gratuitas

&iquest;Est&aacute; preparado para formar parte de un equipo que cambiar&aacute; el futuro del tratamiento del c&aacute;ncer?
&Uacute;nase a nosotros en nuestra misi&oacute;n de vencer al c&aacute;ncer, ensayo cl&iacute;nico a ensayo. Su experiencia y dedicaci&oacute;n pueden ayudarnos a llevar esperanza y curaci&oacute;n a pacientes de todo el mundo. Env&iacute;a tu solicitud en l&iacute;nea.]]></description>
      <pubDate>Tue, 03 Mar 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Enfermero/a de Investigación - Study Coordinator - Barcelona, ES-B]]></title>
      <link>https://j.brt.mv/jb.do?reqGK=27772687&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>4f8376bf-9f85-42a5-aec8-c8de1c61dc51</guid>
      <description><![CDATA[START Center for Cancer Research (&ldquo;START&rdquo;) es la mayor red mundial de centros de fase I, dedicada por completo a la investigaci&oacute;n cl&iacute;nica oncol&oacute;gica. A lo largo de nuestra historia, START ha proporcionado esperanza a pacientes con c&aacute;ncer en consultas de comunidades globales, ofreci&eacute;ndoles acceso a ensayos de vanguardia en Estados Unidos y Europa. En la actualidad, con m&aacute;s de 1.300 estudios realizados y con centros de investigaci&oacute;n en Estados Unidos y en Espa&ntilde;a, Portugal e Irlanda, la misi&oacute;n de START es acelerar el desarrollo de nuevos medicamentos contra el c&aacute;ncer que mejoren la calidad de vida y la supervivencia de los pacientes con c&aacute;ncer y conduzcan a su eventual curaci&oacute;n. Hasta la fecha, m&aacute;s de 43 terapias realizadas en centros START han obtenido la aprobaci&oacute;n de la FDA/EMA.
Vacante disponible: Enfermero/a de Investigaci&oacute;n - Study Coordinator
Responsabilidades:

Identificar los requisitos de los Ensayos cl&iacute;nicos Fase I, incluyendo objetivos, cohortes y necesidades en el cuidado del paciente. 
Asegurar la validez de los datos obtenidos en los documentos fuente
Cumplir con la pol&iacute;tica de env&iacute;os y manipulaci&oacute;n de muestras biol&oacute;gicas
Proporcionar toda la informaci&oacute;n necesaria sobre el ensayo cl&iacute;nico desde el inicio del mismo, as&iacute; como enmiendas posteriores al resto del equipo de investigaci&oacute;n. 
Participar en las Visitas de Inicio.
Realizar todos los trainings que sean necesarios para poner en marcha el ensayos cl&iacute;nico en la Unidad.
Educar al paciente sobre los procedimientos y efectos secundarios relacionados con el ensayo cl&iacute;nico y el/los f&aacute;rmaco/sen investigaci&oacute;n.
Asegurar que el proceso de obtenci&oacute;n del consentimiento informado cumple con las normativas de la AEMPS, GCP, promotor y CEIm
Colaborar con el Investigador para determinar la elegibilidad de un paciente para participar en un ensayo cl&iacute;nico, incluyendo la documentaci&oacute;n necesaria con los criterios de inclusi&oacute;n/exclusi&oacute;n que especifica el protocolo
Garantizar la adhesi&oacute;n al esquema del protocolo de los eventos y requerimientos (queries).
Realizar las llamadas de seguimiento/seguridad/supervivencia a los pacientes seg&uacute;n protocolo, una vez el paciente finalice el tratamiento en ensayo, durante el periodo que se requiera seg&uacute;n protocolo.

Requisitos:

Titulaci&oacute;n de Enfermer&iacute;a
Inter&eacute;s en el &aacute;mbito sanitario
Persona proactiva y con capacidad de organizaci&oacute;n.
Excelente responsabilidad y atenci&oacute;n al detalle
Habilidad para trabajar en equipo y mantener una buena comunicaci&oacute;n con los compa&ntilde;eros y supervisores.
Nivel de ingl&eacute;s intermedio.

&iquest;Est&aacute; preparado para formar parte de un equipo que cambiar&aacute; el futuro del tratamiento del c&aacute;ncer?
&Uacute;nete a nosotros en nuestra misi&oacute;n de vencer al c&aacute;ncer, ensayo cl&iacute;nico a ensayo. Tu experiencia y dedicaci&oacute;n pueden ayudarnos a llevar esperanza y curaci&oacute;n a pacientes de todo el mundo. Env&iacute;a tu solicitud en l&iacute;nea.]]></description>
      <pubDate>Tue, 03 Mar 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Pharmacy Technician - Lake Success,, NY]]></title>
      <link>https://j.brt.mv/jb.do?reqGK=27772632&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>f8ee8279-b300-4535-b92a-3c661a90f811</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largestearly phasesite network, fully dedicated tooncologyclinical research.Throughout ourhistory, START has provided hope to cancer patients inglobalcommunity practices by offering"Hope Through Access&rdquo;tocutting edgetrials throughout the UnitedStatesand Europe. 

The Pharmacy Technician will assure safe, efficient, and cost-effective preparation of chemotherapy, biologic therapy, and supportive care medications for administration to patients following all applicable regulations. Also, this role will work collaboratively with Site Leaders and Pharmacists to maintain adequate and cost-effective inventory of drugs and supplies. The hourly rate for this role is $28 -$31/hour. Your compensation may vary based on your unique qualifications, experience, and market factors.
Work Schedule: 7:30 am-4:00 pm EST
Location: 450 Lakeville Road, Entrance A, Lake Success, NY 11042
Essential Responsibilities

Mix and label chemotherapy, biologic therapy and supportive care medications. 
Perform proper procedures and documentation in inventory management systems during the fulfillment of the medication order. 
Prepare parenteral dosage forms utilizing aseptic techniques in accordance with departmental policies, standards set forth in current USP, state & federal regulations and GCP guidelines for investigational medications. 
Prepare and deliver medication ensuring proper storage location requirements are met based on the stability needs of the product. 
Perform routine weekly inventory and quality assurance tasks, including checking extemporaneously manufactured medications, commercially available medications, I.V. solutions and equipment for expiration dates, recalls, or signs of deterioration. 
Receive medication and supplies in accordance with inventory control and purchasing policies. Help to maintain all medication inventory levels within the predetermined stocking level, calling attention to needs for revision, or perpetual supply problems. 
Interact with study monitors by providing drug accountability reports and temperature storage logs. Facilitate monitor verification of inventory, training and other GCP documentation. 
Maintain and generate reports through the applicable computer programs.  

 Education & Experience

High School Diploma/GED. 
At least 2 years of experience preparing chemotherapy and biologic therapies. 
Current State registration as a pharmacy technician (CPhT). 

 Physical & Travel Requirements:

80% of time spent standing and/or walking. 
Ability to lift up to a 25-pound weight load.Some lifting and bending, pushing and/or pulling loads. 


Best-in-Class Benefits and Perks
We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package&mdash;based on experience&mdash;along with comprehensive benefits designed to support you both personally and professionally: 




 


401(k) retirement savings plan with employer match 






Eligibility for an annual performance bonus, based on role and company results 






Generous paid time off and paid holidays 






Comprehensive medical, dental, and vision coverageand optional insuranceoptions 






Company  paid life and disability insurance for added financial protection 






Employee Assistance Program (EAP) providing confidential, no cost support for you and your family from day one 








Flexible FSA and HSA plans to support your financial wellness 






Commitment to a supportive environment that values balance, wellbeing, and flexibility 






We&rsquo;recommitted to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START,you&rsquo;lljoin a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation. 







More about START
START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. STARTrepresentsthe world&rsquo;s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of &ldquo;Hope Through Access&rdquo;.As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash;one ofthe most effective cancerdrugsin medical history. 

Learn more atSTARTresearch.com. 


Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Tue, 03 Mar 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Técnico de selección (Temporal) - Madrid, ES-M]]></title>
      <link>https://j.brt.mv/jb.do?reqGK=27772693&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>d8677c23-8f0f-4210-ae57-3d7f9b5a4894</guid>
      <description><![CDATA[START Center for Cancer Research (&ldquo;START&rdquo;) es la mayor red mundial de centros de fase I, dedicada por completo a la investigaci&oacute;n cl&iacute;nica oncol&oacute;gica. A lo largo de nuestra historia, START ha proporcionado esperanza a pacientes con c&aacute;ncer en consultas de comunidades globales, ofreci&eacute;ndoles acceso a ensayos de vanguardia en Estados Unidos y Europa. En la actualidad, con m&aacute;s de 1.300 estudios realizados y con centros de investigaci&oacute;n en Estados Unidos y en Espa&ntilde;a, Portugal e Irlanda, la misi&oacute;n de START es acelerar el desarrollo de nuevos medicamentos contra el c&aacute;ncer que mejoren la calidad de vida y la supervivencia de los pacientes con c&aacute;ncer y conduzcan a su eventual curaci&oacute;n. Hasta la fecha, m&aacute;s de 43 terapias realizadas en centros START han obtenido la aprobaci&oacute;n de la FDA/EMA.
Vacante disponible: T&eacute;cnico de Selecci&oacute;n (Temporal con posibilidad a indefinido)
Responsabilidades:

Colaborar con los directores para atraer y reclutar talento de alto nivel, construyendo relaciones s&oacute;lidas que permitan comprender las necesidades de selecci&oacute;n.
Impulsar proactivamente los procesos de selecci&oacute;n para cubrir las vacantes en el menor tiempo posible.
Adoptar un enfoque estrat&eacute;gico en la construcci&oacute;n y mantenimiento de un s&oacute;lido pipeline de talento, utilizando networking y redes sociales para conectar con candidatos altamente calificados.
Garantizar una experiencia excepcional para el candidato desde el primer contacto hasta la negociaci&oacute;n de la oferta, mediante una comunicaci&oacute;n clara, efectiva y orientada al servicio.
Desarrollar estrategias de atracci&oacute;n efectivas para reducir la dependencia de agencias externas, aprovechando informaci&oacute;n del mercado para optimizar los procesos de b&uacute;squeda.
Monitorear continuamente tendencias y mejores pr&aacute;cticas del sector, adaptando los enfoques para fortalecer la atracci&oacute;n y selecci&oacute;n de talento.
Medir y analizar indicadores clave de selecci&oacute;n, proporcionando a los directores informaci&oacute;n y reportes peri&oacute;dicos que faciliten la toma de decisiones y optimicen el proceso de contrataci&oacute;n.
Asegurar que todas las actividades de selecci&oacute;n cumplan con las leyes, regulaciones aplicables y los est&aacute;ndares organizacionales.
Colaborar con el equipo de Talent Acquisition para implementar procesos estandarizados y compartir mejores pr&aacute;cticas.
Gestionar relaciones con socios externos y proveedores que apoyen los objetivos de Talent Acquisition.

Educaci&oacute;n y experiencia requeridas:

Licenciatura en Administraci&oacute;n de Empresas, Recursos Humanos, Psicolog&iacute;a o carrera af&iacute;n.
Experiencia en selecci&oacute;n de ciclo completo en entornos din&aacute;micos y de ritmo acelerado.
Experiencia en adquisici&oacute;n de talento dentro de la industria farmac&eacute;utica, CRO, biotecnolog&iacute;a y/o sector salud.
Ingles avanzado (indispensable)
Se valorar&aacute; positivamente el conocimiento de otro idioma.

Beneficios

Jornada de Lunes a Viernes (Festivos y Fines de Semana libres)
30 d&iacute;as laborables de vacaciones
Retribuci&oacute;n flexible
Posibilidad de realizar clases particulares de ingl&eacute;s totalmente gratuitas

&iquest;Est&aacute; preparado para formar parte de un equipo que cambiar&aacute; el futuro del tratamiento del c&aacute;ncer?
&Uacute;nase a nosotros en nuestra misi&oacute;n de vencer al c&aacute;ncer, ensayo cl&iacute;nico a ensayo. Su experiencia y dedicaci&oacute;n pueden ayudarnos a llevar esperanza y curaci&oacute;n a pacientes de todo el mundo. Env&iacute;a tu solicitud en l&iacute;nea.]]></description>
      <pubDate>Tue, 03 Mar 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Patient Navigator - Madrid, ES-M]]></title>
      <link>https://j.brt.mv/jb.do?reqGK=27772690&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>36ef74ce-0df2-45c4-bfa9-6a5040e17b4d</guid>
      <description><![CDATA[START Center for Cancer Research (&ldquo;START&rdquo;) es la mayor red mundial de centros de fase I, dedicada por completo a la investigaci&oacute;n cl&iacute;nica oncol&oacute;gica. A lo largo de nuestra historia, START ha proporcionado esperanza a pacientes con c&aacute;ncer en consultas de comunidades globales, ofreci&eacute;ndoles acceso a ensayos de vanguardia en Estados Unidos y Europa. En la actualidad, con m&aacute;s de 1.300 estudios realizados y con centros de investigaci&oacute;n en Estados Unidos y en Espa&ntilde;a, Portugal e Irlanda, la misi&oacute;n de START es acelerar el desarrollo de nuevos medicamentos contra el c&aacute;ncer que mejoren la calidad de vida y la supervivencia de los pacientes con c&aacute;ncer y conduzcan a su eventual curaci&oacute;n. Hasta la fecha, m&aacute;s de 43 terapias realizadas en centros START han obtenido la aprobaci&oacute;n de la FDA/EMA.
Vacante disponible: Patient Navigator
Responsabilidades:

Realizar la admisi&oacute;n de derivaciones y asistir con la coordinaci&oacute;n entre pacientes y proveedores de salud.
Mantener la documentaci&oacute;n de las derivaciones y monitorear las tendencias de referencia.
Evaluar a los pacientes utilizando sistemas de historia cl&iacute;nica electr&oacute;nica (EMR) y plataformas gen&oacute;micas para determinar su elegibilidad.
Apoyar al/la Enfermero/a en la difusi&oacute;n del programa y la promoci&oacute;n de ensayos cl&iacute;nicos.
Participar en reuniones del programa y contribuir a los esfuerzos de seguimiento de datos.
Otras funciones seg&uacute;n se asignen.

Requisitos

Inter&eacute;s en Ensayos Cl&iacute;nicos
Capacidad creativa para la resoluci&oacute;n de problemas; habilidad para navegar a trav&eacute;s de complejos protocolos oncol&oacute;gicos de fase I y aplicarlos a la misi&oacute;n de START de recopilaci&oacute;n de datos de calidad.
Persona proactiva y con capacidad de organizaci&oacute;n.
Habilidad para trabajar en equipo y mantener una buena comunicaci&oacute;n con los compa&ntilde;eros y supervisores.

Beneficios

Jornada de Lunes a Viernes (Festivos y Fines de Semana libres)
30 d&iacute;as laborables de vacaciones
Retribuci&oacute;n flexible
Posibilidad de realizar clases particulares de ingl&eacute;s totalmente gratuitas

&iquest;Est&aacute; preparado para formar parte de un equipo que cambiar&aacute; el futuro del tratamiento del c&aacute;ncer?
&Uacute;nase a nosotros en nuestra misi&oacute;n de vencer al c&aacute;ncer, ensayo cl&iacute;nico a ensayo. Su experiencia y dedicaci&oacute;n pueden ayudarnos a llevar esperanza y curaci&oacute;n a pacientes de todo el mundo. Env&iacute;a tu solicitud en l&iacute;nea.]]></description>
      <pubDate>Tue, 03 Mar 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Scheduler - Los Angeles, CA]]></title>
      <link>https://j.brt.mv/jb.do?reqGK=27772555&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>ee44f19a-9c39-477a-b994-642c418dd527</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largestearly phasesite network, fully dedicated tooncologyclinical research.Throughout ourhistory, START has provided hope to cancer patients inglobalcommunity practices by offering"Hope Through Access&rdquo;tocutting edgetrials throughout the UnitedStatesand Europe. 
We are seeking a Scheduler, for our Los Angeles, CA location at 10700 Santa Monica, Suite 310, Los Angeles, CA 90025. This role will facilitate excellent patient care by supporting and collaborating with the clinic team. This is a fully on-site role. The hours are 8:00am-5:00pm, Monday through Friday. Some flexibility may be needed based on needs of the clinic.
The hourly rate for this role is $24 - $29/hour. Your compensation may vary based on your unique qualifications, experience, and market factors.
Essential Responsibilities

Manage scheduling for study-specific appointments, radiology procedures, and travel arrangements.
Ensure prior authorizations are completed.
Handle administrative tasks, including follow-ups, referrals, no-shows, and rescheduling.
Maintain accurate electronic medical records and manage documentation.
Communicate with patients and care team members to ensure coordinated care.
Support quality improvement initiatives for efficient, cost-effective care.
Participate in ongoing education and training to maintain skills and competency.

Required Education and Experience: 

High School Diploma or equivalent. 
One year experience in an outpatient physician practice or healthcare setting. 
Effective communication skills and collaborative attitude. 
Strong attention to detail. 
Knowledge of medical terminology as it relates to scheduling study specific procedures such as CT/MRI/PET scans, biopsies, eye exams, etc. 

Preferred Education and Experience: 

Oncology and/or research experience. 

Best-in-Class Benefits and Perks
We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package&mdash;based on experience&mdash;along with comprehensive benefits designed to support you both personally and professionally: 





401(k) retirement savings plan with employer match
Eligibility for an annual performance bonus, based on role and company results
Generous paid time off and paid holidays
Comprehensive medical, dental, and vision coverageand optional insuranceoptions
Company paid life and disability insurance for added financial protection
Employee Assistance Program (EAP) providing confidential, no cost support for you and your family from day one Flexible FSA and HSA plans to support your financial wellness Commitment to a supportive environment that values balance, wellbeing, and flexibility
We&rsquo;re committed to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START, you&rsquo;ll join a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation.

 
More about START
START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. STARTrepresentsthe world&rsquo;s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of &ldquo;Hope Through Access&rdquo;.As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash;one ofthe most effective cancerdrugsin medical history. 
Learn more atSTARTresearch.com. 
Ready to be part of a team changing the future of cancer treatment? Join us in our mission to conquer cancer, one clinical trial at a time. Yourexpertiseand dedication can help us bring hope and healing to patients worldwide.Pleasesubmityour application online. 
We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Mon, 02 Mar 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Financial & Operations Analyst (Remote) - San Antonio, TX]]></title>
      <link>https://j.brt.mv/jb.do?reqGK=27772362&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>b05cf17f-cfe1-46a6-9013-77a6592f3b3d</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering access to cutting edge trials throughout the US and Europe. Today, with over 1,300 studies completed, and with research facilities in the United States and in Spain, Portugal, and Ireland, START&rsquo;s mission is to accelerate the development of new anticancer drugs that will improve the quality of life and survival for patients with cancer and lead to its eventual cure. To date, over 43 therapies conducted at START locations have obtained FDA/EMA approval. Incredibly, while Academic Medical Centers (AMCs) conduct 80% of cancer trials, such trials reach only 20% of the patient population &ndash; leaving the majority of patients who are treated in community practices and hospitals without access to a clinical trial when their care journey calls for one. START serves the many &ndash; by bringing cancer trials to physicians and their patients in community hospitals and practices when hope is needed most.
 
START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash; the most effective cancer drug in medical history.

We are hiring a motivated Financial & Operations Analyst who will report to the Director, Finance &ndash; Operations and play a critical role in strengthening the partnership between Finance and Operations. This role will provide accurate, timely, and actionable insights that support operational efficiency, profitability, and strategic decisionmaking across START&rsquo;s clinic network and joint ventures. The position supports both recurring operational reporting and higher-level strategic analysis during periods of rapid growth and expansion. will be responsible for overseeing the accounts payable process, ensuring accurate and timely processing of invoices, and payments to vendors. 
This is a remote role. The annual base salary for this role is $80,000 - $90,000. However, base pay may vary depending on multiple individualized factors including market location, job-related knowledge, skills, and experience. 
Essential Responsibilities
Capacity Modeling & Operational Analytics
&middot;       Distribute monthly reports highlighting group and individual efficiency, along with variance to benchmark performance.
&middot;       Maintain and continuously improve capacity models across US, EU, Late Phase, Pediatrics, and Central Operations.
&middot;       Advance current models toward greater automation, standardization, and frequency.
&middot;       Analyze clinic throughput, sitelevel performance, and operational bottlenecks to identify improvement opportunities.
Business Reviews & Operational Visibility
&middot;       Prepare monthly and quarterly business review materials for clinics, departments, and sponsorfacing teams (Regulatory, Study StartUp, Procurement, etc.).
&middot;       Prepare analytical packages to support leadership decisionmaking on investments, new sites, resource allocation, and operational improvement initiatives.
Joint Venture (JV) Support & Financial Reporting
&middot;       Prepare monthly and quarterly JV reporting packages, including highlevel metrics, financial statements, and variance analyses.
&middot;       Support JV meetings by ensuring materials are complete, accurate, and delivered on time; attend or run meetings as needed.
&middot;       Respond to partner and internal stakeholder requests for financial data, insights, and analysis.
CrossFunctional Collaboration
&middot;       Serve as a bridge between Finance and Operations, ensuring shared understanding of financial drivers, constraints, and opportunities.
&middot;       Partner with clinic and departmental leaders to identify risks, trends, and areas requiring deeper review. 
&middot;       Support development, enhancement, and maintenance of Power BI dashboards used across Finance and Operations.
&middot;       Other duties may be assigned at any time. 
Required Education and Experience: 
&middot;       Bachelor&rsquo;s degree in Finance, Accounting, Economics, Data Analytics, or related field.
&middot;       2&ndash;5 years of financial analysis, operations analysis, or related analytical experience.
&middot;       Advanced Excel skills; strong proficiency in data modeling and scenario-based analysis.
&middot;       Experience with BI tools (Power BI strongly preferred).
&middot;       Strong attention to detail with the ability to synthesize complex data into clear insights.
&middot;       Ability to manage multiple priorities in a fast-paced, evolving environment.
Preferred Education and Experience:
&middot;       Experience in healthcare, clinical research, or multi-site operational environments.
&middot;       Familiarity with ERP or planning tools (NetSuite, Adaptive Planning).
&middot;       Ability to automate repetitive reporting processes.
&middot;       Comfort interacting with senior leadership and external partners.
Physical & Travel Requirements:
&middot;       Travel: Required to travel up to 20% of the time
&middot;       Sitting: Must be able to sit for extended periods of time. 
&middot;       Standing: Must be able to stand for extended periods of time.  
&middot;       Bending: Must be able to reach overhead, at shoulder level, or bend to perform tasks. 
Best-in-Class Benefits and Perks
We value our employees&rsquo; time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:
&middot;       Comprehensive health coverage: Medical, dental, and vision insurance provided
&middot;       Robust retirement planning: 401(k) plan available with employer matching
&middot;       Financial security: Life and disability insurance for added protection
&middot;       Flexible financial options: Health savings and flexible spending accounts offered
&middot;       Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided
&middot;       Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.

More about The START Center for Cancer Research
Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including for 43 therapies that were approved by the FDA. START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. Learn more at STARTresearch.com.

Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Fri, 27 Feb 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Senior Manager, Study Activation (EU)  - Madrid, ES-M]]></title>
      <link>https://j.brt.mv/jb.do?reqGK=27772255&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>37d6acf3-b30f-48b6-9311-8474b0947dc5</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering access to cutting edge trials throughout the US and Europe. Today, with over 1,300 studies completed, and with research facilities in the United States and in Spain, Portugal, and Ireland, START&rsquo;s mission is to accelerate the development of new anticancer drugs that will improve the quality of life and survival for patients with cancer and lead to its eventual cure.
 
START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash; the most effective cancer drug in medical history.
We are seeking a Senior Manager, Study Activation (EU) 


Essential Responsibilities:  




Supports SSU strategy in close collaboration with the VP, Client Engagement & Study Activation 






Collaborates with central services and site-level study team to ensure SSU timelines and deliverables are met according to internal process, KPIs, and Sponsor goals 






Accountable for timely start-up activities until Green Light (ready to initiate site millstone)  






Supports study feasibility and site selection milestones in close collaboration with Pre-Award Team as well as the site-level study team. 






Supports and directs all study activation milestones in close collaboration with Study Start-up Specialist as well as the site-level study team. 






Serves as main contact for issues in SSU phases, escalating as necessary 






Ensures sites are prepared for "Green Light" and ensures all documentation is in place for initial and subsequent drug release. Responsible for review and sign off of the site "Green Light" 






Oversees EU SSU team activities to achieve start-up timelines and quality execution, (proposing and implementing corrective actions where appropriate), according to START standards  






Leads EU SSU team meetings and participates in network study team meetings, as required 






Contribute to the growth and development of departmental staff, processes and systems. 






Ability to embrace HubSpot, Veeva Vault, FileMaker, and CTMS system and associated functionality and maintain records related to specific area of assignment 








Assist with in-service trainings and new hire trainings for staff 






Assist with special projects as assigned.  This includes, but is not limited to, conducting research, preparing presentations and documents as requested 






Serves as a back to the VP and departmental team, when needed 






Perform additional duties as assigned 




Required Education and Experience: 




BA/BS degree with at least 5 years of experience in pharmaceutical related drug development or direct equivalent experience or advanced degree   






Must have knowledge of clinical trial conduct, including, multi-center, global trials. 






Experience within the EU-CTR 






Must have strong knowledge of ICH/GCP guidelines and regulatory requirements.  






Requires proven project management skills and leadership ability  






Must have excellent interpersonal, written and verbal communication skills, administrative skills and computer ability.  






Experience in working cross functionally and with external providers  






Experience with development & implementation of process improvement related initiatives  






Global Experience with site activation activities including submission requirements.  




Travel Requirements: 




Travel: Required to travel up to 20% of the time  






Approximately 80% of time is spent sitting. 






Very fast-paced and ever-changing healthcare environment. 








Demanding deadlines and time frames. 






Constant demand for updating knowledge 




 Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.]]></description>
      <pubDate>Wed, 25 Feb 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Auxiliar Administrativo (Temporal) - Sector Sanitario - Madrid, ES-M]]></title>
      <link>https://j.brt.mv/jb.do?reqGK=27771852&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>96f956c9-3ce3-4e29-b53c-8439f487a2ad</guid>
      <description><![CDATA[START Center for Cancer Research (&ldquo;START&rdquo;) es la mayor red mundial de centros de fase I, dedicada por completo a la investigaci&oacute;n cl&iacute;nica oncol&oacute;gica. A lo largo de nuestra historia, START ha proporcionado esperanza a pacientes con c&aacute;ncer en consultas de comunidades globales, ofreci&eacute;ndoles acceso a ensayos de vanguardia en Estados Unidos y Europa. En la actualidad, con m&aacute;s de 1.300 estudios realizados y con centros de investigaci&oacute;n en Estados Unidos y en Espa&ntilde;a, Portugal e Irlanda, la misi&oacute;n de START es acelerar el desarrollo de nuevos medicamentos contra el c&aacute;ncer que mejoren la calidad de vida y la supervivencia de los pacientes con c&aacute;ncer y conduzcan a su eventual curaci&oacute;n. Hasta la fecha, m&aacute;s de 43 terapias realizadas en centros START han obtenido la aprobaci&oacute;n de la FDA/EMA.
Vacante disponible: Auxiliar Administrativo
Responsabilidades:

Proteger la confidencialidad del paciente y del protocolo, aplicando los requisitos necesarios de protecci&oacute;n de datos del paciente.
Atenci&oacute;n al paciente tanto por tel&eacute;fono como en el mostrador solucionando todas las dudas que puedan surgir y derivando a la enfermera de investigaci&oacute;n si as&iacute; es requerido.
Citar a los pacientes para todas las visitas y procedimientos que requiere el ensayo cl&iacute;nico en el que participa tanto en eMR como en el sistema inform&aacute;tico del hospital, mantener actualizados los esquemas de procedimientos de los pacientes y llevar el control de los huecos disponibles en la sala de tratamiento.
Fotocopiar/escanear los informes de los pacientes externos si as&iacute; es requerido (generalmente cuando los pacientes son firmes candidatos a un ensayo &oacute; han firmado CI). Informar a los pacientes de las citas.
Recepcionar y mentener registro de las muestras de AP para procesado de determinaciones de biolog&iacute;a molecular o env&iacute;o a sponsor. Escanear el informe de Anatom&iacute;a Patol&oacute;gica para nuestros archivos electr&oacute;nicos.
Gesti&oacute;n de agendas de los m&eacute;dicos de la Unidad de Ensayos Fase I.
Gesti&oacute;n de documentaci&oacute;n electr&oacute;nica y en papel para el mantenimiento de la historia m&eacute;dica electr&oacute;nica eMR.
Participar en el proceso de gastos de reembolsos de pacientes.

Requisitos

Inter&eacute;s en Ensayos Cl&iacute;nicos
Capacidad creativa para la resoluci&oacute;n de problemas; habilidad para navegar a trav&eacute;s de complejos protocolos oncol&oacute;gicos de fase I y aplicarlos a la misi&oacute;n de START de recopilaci&oacute;n de datos de calidad.
Persona proactiva y con capacidad de organizaci&oacute;n.
Habilidad para trabajar en equipo y mantener una buena comunicaci&oacute;n con los compa&ntilde;eros y supervisores.

Jornada

Jornada completa de Lunes a Viernes
Horario: 14:30 a 22:00
Contrato temporal: Sustituci&oacute;n de una baja m&eacute;dica

&iquest;Est&aacute; preparado para formar parte de un equipo que cambiar&aacute; el futuro del tratamiento del c&aacute;ncer?
&Uacute;nase a nosotros en nuestra misi&oacute;n de vencer al c&aacute;ncer, ensayo cl&iacute;nico a ensayo. Su experiencia y dedicaci&oacute;n pueden ayudarnos a llevar esperanza y curaci&oacute;n a pacientes de todo el mundo. Env&iacute;e su solicitud en l&iacute;nea.]]></description>
      <pubDate>Thu, 19 Feb 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Infusion Nurse - Los Angeles, CA]]></title>
      <link>https://j.brt.mv/jb.do?reqGK=27771110&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>48884f4c-2408-4f67-8823-16dae40207fa</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering access to cutting edge trials throughout the US and Europe. Today, with over 1,300 studies completed, and with research facilities in the United States and in Spain, Portugal, and Ireland, START&rsquo;s mission is to accelerate the development of new anticancer drugs that will improve the quality of life and survival for patients with cancer and lead to its eventual cure. To date, over 43 therapies conducted at START locations have obtained FDA/EMA approval. Incredibly, while Academic Medical Centers (AMCs) conduct 80% of cancer trials, such trials reach only 20% of the patient population &ndash; leaving the majority of patients who are treated in community practices and hospitals without access to a clinical trial when their care journey calls for one. START serves the many &ndash; by bringing cancer trials to physicians and their patients in community hospitals and practices when hope is needed most.
 
START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash; the most effective cancer drug in medical history.

We are hiring an Infusion Nurse who will be responsible for providing direct patient care to individuals who are participants in research protocols that are conducted at START. The Infusion Nurse uses appropriate professional judgment and decision-making in planning and providing care. Nursing care is to be delivered in a manner consistent with the Standard Operating Procedures and standards of practice, and professional evidence-based standards.
This position is offered at a pay range of $60.00 to $80.00 per hour, based on experience, qualifications, and internal equity. In addition, employees in this role may be eligible for an annual bonus of up to 10% of base earnings.
Essential Responsibilities
Patient Care

Administer chemotherapy/immunotherapy/investigational agent to participants (inclusive of parenteral) according to the protocol and applicable regulations.
Perform study-related activities including but not limited to venipuncture, obtaining blood specimens, IV insertion, and venous access device (central line) management, ECG collection, and vital signs.
Collect biological samples according to the protocol and Standard Operating Procedures.
Educate, explain, and inform participants of study procedures.
Record data obtained according to the protocol and Standard Operating Procedures.
Use nursing assessment skills to observe participant general well-being and potential adverse events. Document events and take appropriate action as needed.
Respond to emergency situations based upon nursing standards.
Provide patient education regarding participation in a clinical trial, chemotherapy/immunotherapy/investigational agent administration and potential side effects.
Ensure that the dignity, health, safety, and welfare of participants are given the highest priority at all times.

Planning and problem solving tasks

Prepare for clinic day ensuring necessary supplies.
Assist with entry and completion of quality standards for EHR/PQRS.

Communicating tasks

Assist with the training and mentorship of less tenured staff.
Communicate with providers regarding a change in patient status.
Communicate and interact with peers and other departments in a manner that is viewed as having a positive eect on patient services and sta morale. Interact eectively with patients/family members and demonstrate sensitivity in regards to cultural diversity, age specic needs and condentiality.

Protocol Management tasks

Work with study team to ensure that study related procedures, drug administration, labs, vital signs and ECG are completed. 

Technical and Quality Tasks

Use skills, knowledge, nursing diagnosis, and clinical judgement in order to provide a high standard of care for participants in clinical trials.
Remain current with appropriate emergency certifications and company emergency policy and procedures.
Able to work effectively and efficiently under tight deadlines, high volumes and multiple interruptions.
Other duties may be assigned at any time.


Education & Experience

High School Diploma or GED.
Licensed Registered Nurse in practicing state.
Basic Life Support (BLS) certification, and AHA certified program. 
Previous experience in peripheral IV insertion and management of venous access device(s).   


Preferred Education and Experience:

1 year of experience.
Oncology Certified Nurse (OCN).
Clinical Trial and oncology experience.
Experience working with Microsoft Office, including Teams, Excel and Word. 
Advanced Cardiac Life Support (ACLS) Certification, an AHA certified program.  Can be obtained within 90 days of hire. 
ONS/ONCC Chemotherapy Immunotherapy Certificate&trade;.  Can be obtained within first year of employment.

Physical & Travel Requirements:

80% of time spent standing and/or walking.
Ability to lift up to a 60-pound weight load.
Very frequent lifting and bending, pushing and/or pulling loads.
Able to perform manual tasks that require the use of ne muscle motor skills.


Best-in-Class Benefits and Perks
We value our employees&rsquo; time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:

Comprehensive health coverage: Medical, dental, and vision insurance provided
Robust retirement planning: 401(k) plan available with employer matching
Financial security: Life and disability insurance for added protection
Flexible financial options: Health savings and flexible spending accounts offered
Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided

Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.

More about The START Center for Cancer Research
Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including for 43 therapies that were approved by the FDA. START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. Learn more at STARTresearch.com.

Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Tue, 10 Feb 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[In Vivo Research Assistant - San Antonio, TX]]></title>
      <link>https://j.brt.mv/jb.do?reqGK=27771057&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>69712592-2f0c-4739-8b6a-950351cc574b</guid>
      <description><![CDATA[XenoSTART, the preclinical division of START is a translational research organization focused on creating relevant preclinical cancer models.  Our xenograft models represent each cancer type and disease stage and are established from patients at our domestic and international cancer centers. The XenoSTART Patient-Derived Xenograft (XPDX) platform includes over 2,500 models annotated with each donor patient&rsquo;s cancer treatment and outcome data and characterized using IHC, DNA/RNA sequencing, and relevant in vivo drug efficacy.
Our XPDX models are clinically annotated and include patient treatment history and outcome and are characterized through genomic profiling, histologic analysis, and in vivo drug sensitivity to relevant standards of care. These models may be utilized in the following manner:
In vivo PK/PD and efficacy studies

In vivo efficacy panel screens (indication or target focused)
In licensing of models for internal studies
Custom model development
Orthotopic and radiotherapy studies
Ex vivo and organoid studies

 We are hiring a motivated In Vivo Research Assistant.  Under direct supervision of the supervisor, this position involves collection of data obtained from industry sponsored and investigator-initiated studies. In addition, this position entails all procedures involved with small animal handling, husbandry, surgery, drug preparation and dosing and other related duties for the START Preclinical Group.
Essential Responsibilities

Collect internally generated data including small animal body weights and tumor dimensions using mechanical and electronic devices and stores on internal server. 
Perform day-to-day procedures including but not limited to small animal handling, husbandry, surgery, anesthesia, cell culture, blood and tissue collection and processing, tumor implantation, cell injection, euthanasia, sample processing including cryopreservation, cryofreezing and fixation, sterilization, maintenance and cleaning. These operations may involve multi-tasking, lifting of greater than forty pounds, standing or sitting for long periods of time and repetitive procedures. 
Prepare, aliquot and properly store vehicles, drugs, media and other laboratory solutions. 
Administer agents by various routes on various dosing schedules. 
Attend regular meetings and briefings regarding preclinical studies as required. 
Assist in animal and laboratory activities as needed. 
Assist in data preparation and administrative log management as needed. 
Follow all Standard Operating Procedures (SOPs). 

Education & Experience

High school diploma/GED.
Minimum of 1 year of similar experience.
Must be familiar with Microsoft Office applications.
Attention to detail.
Ability to work in a fast-paced team environment.

Preferred Education and Experience:

Bachelor&rsquo;s degree.
Knowledge and training in animal handling and research.

Best-in-Class Benefits and Perks
We value our employees&rsquo; time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:

Comprehensive health coverage: Medical, dental, and vision insurance provided
Robust retirement planning: 401(k) plan available with employer matching
Financial security: Life and disability insurance for added protection
Flexible financial options: Health savings and flexible spending accounts offered
Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided
Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.


More about The START Center for Cancer Research
Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including for 43 therapies that were approved by the FDA. START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. Learn more at STARTresearch.com.

Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.

We are an equal opportunity employer that welcomes and encourages diversity]]></description>
      <pubDate>Mon, 09 Feb 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Enfermero/a - Oncología - La Rioja, LO]]></title>
      <link>https://j.brt.mv/jb.do?reqGK=27770757&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>7f1279d5-92ea-4a00-a995-94c1d6b39e81</guid>
      <description><![CDATA[START Center for Cancer Research (&ldquo;START&rdquo;) es la mayor red mundial de centros de fase I, dedicada por completo a la investigaci&oacute;n cl&iacute;nica oncol&oacute;gica. A lo largo de nuestra historia, START ha proporcionado esperanza a pacientes con c&aacute;ncer en consultas de comunidades globales, ofreci&eacute;ndoles acceso a ensayos de vanguardia en Estados Unidos y Europa. En la actualidad, con m&aacute;s de 1.300 estudios realizados y con centros de investigaci&oacute;n en Estados Unidos y en Espa&ntilde;a, Portugal e Irlanda, la misi&oacute;n de START es acelerar el desarrollo de nuevos medicamentos contra el c&aacute;ncer que mejoren la calidad de vida y la supervivencia de los pacientes con c&aacute;ncer y conduzcan a su eventual curaci&oacute;n. Hasta la fecha, m&aacute;s de 43 terapias realizadas en centros START han obtenido la aprobaci&oacute;n de la FDA/EMA.
Vacante disponible: Enfermero/a de Tratamiento- Ensayos Cl&iacute;nicos Oncol&oacute;gicos
Responsabilidades:

Promover el cumplimiento de los procedimientos necesarios requeridos por el ensayo cl&iacute;nico.
Colaborar con el equipo de investigaci&oacute;n para mejorar los procedimientos realizados al paciente desde su inclusi&oacute;n hasta la finalizaci&oacute;n del ensayo cl&iacute;nico.
Tomar las constantes vitales, peso, talla y realizar todos los procedimientos necesarios requeridos por el protocolo del ensayo cl&iacute;nico.
Administrar los tratamientos de acuerdo con el protocolo y los requisitos normativos.
Recoger muestras de sangre, suero y/u orina de los pacientes para el laboratorio cl&iacute;nico seg&uacute;n lo requiera el protocolo.
Extraer, procesar y enviar muestras de Farmacocin&eacute;tica (PK)/Farmacodinamia.

Requisitos

Inter&eacute;s en Ensayos Cl&iacute;nicos
Capacidad creativa para la resoluci&oacute;n de problemas; habilidad para navegar a trav&eacute;s de complejos protocolos oncol&oacute;gicos de fase I y aplicarlos a la misi&oacute;n de START de recopilaci&oacute;n de datos de calidad.
Persona proactiva y con capacidad de organizaci&oacute;n.
Habilidad para trabajar en equipo y mantener una buena comunicaci&oacute;n con los compa&ntilde;eros y supervisores.

Formaci&oacute;n

Licenciatura en Enfermer&iacute;a
Colegiatura en Enfermer&iacute;a

&iquest;Est&aacute; preparado para formar parte de un equipo que cambiar&aacute; el futuro del tratamiento del c&aacute;ncer?
&Uacute;nase a nosotros en nuestra misi&oacute;n de vencer al c&aacute;ncer, ensayo cl&iacute;nico a ensayo. Su experiencia y dedicaci&oacute;n pueden ayudarnos a llevar esperanza y curaci&oacute;n a pacientes de todo el mundo. Env&iacute;e su solicitud en l&iacute;nea.]]></description>
      <pubDate>Tue, 03 Feb 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Study Activation - Clinical Trials (Temporal) - Madrid, ES-M]]></title>
      <link>https://j.brt.mv/jb.do?reqGK=27770651&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>6734c403-b08f-4181-ae3f-12d3eb2b1587</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering access to cutting edge trials throughout the US and Europe. Today, with over 1,300 studies completed, and with research facilities in the United States and in Spain, Portugal, and Ireland, START&rsquo;s mission is to accelerate the development of new anticancer drugs that will improve the quality of life and survival for patients with cancer and lead to its eventual cure. To date, over 43 therapies conducted at START locations have obtained FDA/EMA approval. Incredibly, while Academic Medical Centers (AMCs) conduct 80% of cancer trials, such trials reach only 20% of the patient population &ndash; leaving the majority of patients who are treated in community practices and hospitals without access to a clinical trial when their care journey calls for one. START serves the many &ndash; by bringing cancer trials to physicians and their patients in community hospitals and practices when hope is needed most.
 
START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash; the most effective cancer drug in medical history.

We are hiring a: Pre &ndash; Award Coordinator (Study Activation)

Essential Responsibilities:

Perform all pre-award activities from time of initial contact to official site selection for the START Europe sites.
Review, respond, and maintain the central email inbox for new study opportunities.
Facilitate all pre-award related meetings, including but not limited to, Protocol Review and Development Committee meetings, Pre-Study Site Visits, weekly Study Start-Up Status meetings, and Sponsor/Investigator meetings for the START Europe sites.
Coordinate facility tours prior to official site selection.
Support execution of the Sponsor/CRO required site feasibility questionnaires for the START Europe sites when applicable and ensuring the questionnaire are completed accurately and in a timely manner.
Work within the forecasted timelines in accordance with Sponsor/CRO expectations and ensure they are met; if forecasted timelines are not reached, provide clear rationale for delays and contingency plans to mitigate impact.
Review and comply with Standard Operating Procedures and pre-award processes in a timely manner and ensure all relevant documents are submitted to Sponsor/CRO and the Investigational Site File (ISF).
Anticipate and identify issues during pre-award process, resolve minor to moderate issues independently, and escalate complex issues.


Maintain and ensure data tracking systems are updated with pre-award milestones.
Assist with in-service trainings and new hire trainings for staff.
Assist with special projects as assigned.  This includes, but is not limited to, conducting research, preparing presentations and documents as requested.


Other duties may be assigned at any time.


Required Education and Experience:

High school diploma or equivalent.
At least two years&rsquo; experience in administrative setting Proficient working knowledge of word processing, spreadsheet, database, and presentation software (MS Office skills such as Outlook, Word, Excel, PowerPoint, and SharePoint).
Excellent written and oral communication skills, as well as time management skills.
Demonstrated ability to work in a dynamic environment under compressed deadlines across several projects, each with unique requirements.



More about The START Center for Cancer Research
Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including for 43 therapies that were approved by the FDA. START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. Learn more at STARTresearch.com.

Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Mon, 02 Feb 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Scheduler - West Valley City, UT]]></title>
      <link>https://j.brt.mv/jb.do?reqGK=27770470&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>d1d1f695-d192-48bf-b8d5-ddb7819e7177</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering access to cutting edge trials throughout the US and Europe. Today, with over 1,300 studies completed, and with research facilities in the United States and in Spain, Portugal, and Ireland, START&rsquo;s mission is to accelerate the development of new anticancer drugs that will improve the quality of life and survival for patients with cancer and lead to its eventual cure. To date, over 43 therapies conducted at START locations have obtained FDA/EMA approval. Incredibly, while Academic Medical Centers (AMCs) conduct 80% of cancer trials, such trials reach only 20% of the patient population &ndash; leaving the majority of patients who are treated in community practices and hospitals without access to a clinical trial when their care journey calls for one. START serves the many &ndash; by bringing cancer trials to physicians and their patients in community hospitals and practices when hope is needed most.
START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash; the most effective cancer drug in medical history.
We are hiring a Scheduler, for our West Valley City, Utah location at 2965 W 3500 S, West Valley City, UT 84119. This role will facilitate excellent patient care by supporting and collaborating with the clinic team. This is a fully on-site role. The hours are 7:00am-3:30pm, Monday through Friday. Some flexibility may be needed based on needs of the clinic.
The hourly rate for this role is $20 - $25/hour + annual performance bonus opportunity. Your compensation may vary based on your unique qualifications, experience, and market factors.
Essential Responsibilities

Manage scheduling for study-specific appointments, radiology procedures, and travel arrangements.
Ensure prior authorizations are completed.
Handle administrative tasks, including follow-ups, referrals, no-shows, and rescheduling.
Maintain accurate electronic medical records and manage documentation.
Communicate with patients and care team members to ensure coordinated care.
Support quality improvement initiatives for efficient, cost-effective care.
Participate in ongoing education and training to maintain skills and competency.

Required Education and Experience: 

High School Diploma or equivalent. 
One year experience in an outpatient physician practice or healthcare setting. 
Effective communication skills and collaborative attitude. 
Strong attention to detail. 
Knowledge of medical terminology as it relates to scheduling study specific procedures such as CT/MRI/PET scans, biopsies, eye exams, etc. 

Preferred Education and Experience: 

Oncology and/or research experience. 

Best-in-Class Benefits and Perks
We value our employees&rsquo; time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:

Comprehensive health coverage: Medical, dental, and vision insurance provided
Robust retirement planning: 401(k) plan available with employer matching
Financial security: Life and disability insurance for added protection
Flexible financial options: Health savings and flexible spending accounts offered
Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided
Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.

More about The START Center for Cancer Research
Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including 43 therapies that were approved by the FDA. START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. Learn more at STARTresearch.com.
Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.
We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Fri, 30 Jan 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Clinical Trainer, Integrations (Remote) - San Antonio, TX]]></title>
      <link>https://j.brt.mv/jb.do?reqGK=27769809&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>6bcfe048-4e48-4837-926b-ba2f70ebd045</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. To date, over 45 therapies conducted at START locations have obtained FDA/EMA approval. 
The START Center for Cancer Research is seeking a Clinical Trainer, Integrations to join the Integration team and lead the rollout of new START locations in the US and internationally. This role is responsible for managing the end-to-end integration process for new clinical sites, with a particular emphasis on onboarding and training all new clinical team members&mdash;including nursing, research coordinators, and scheduling teams. The Clinical Trainer will collaborate closely with Operations, Training, Quality Assurance and other central service departments to ensure seamless site launches, consistent high-quality patient care, and adherence to project timelines and standards.
The ideal candidate will demonstrate strong project management skills, experience with onboarding and training multidisciplinary teams, and proficiency with project management tools and regular progress reporting.
This is a remote role. The annual base salary for this role is $80,000 - $120,000. However, base pay may vary depending on multiple individualized factors including market location, job-related knowledge, skills, and experience. A 10% annual performance bonus is offered as well.
Essential Responsibilities

Lead the planning, coordination and execution of clinical training for each new early-phase clinical oncology research location
Collaborate closely with Training and Quality departments to build comprehensive onboarding and training programs for all new clinical team members, including nursing, research coordinators and scheduling staff
Oversee and facilitate onboarding and training programs for clinical team members for new sites
Develop and document new clinical workflows as needed and incorporate into training
Develop and implement project plans, timelines, and deliverables, ensuring all integration milestones are met
Utilize project management tools to track progress, manage tasks, and generate regular status reports for leadership and stakeholders
Monitor and report on integration progress, identifying risks and proactively addressing challenges to ensure successful site launches
Collaborate with leadership and multidisciplinary teams to ensure operational readiness and alignment with organizational goals
Travel to new and existing START locations to oversee onboarding, training, and process implementation

Education & Experience

Education: Bachelor&rsquo;s degree in a healthcare, science, business, or related field. RN license is a plus but not required
Certifications: Project management certification (e.g., PMP, CAPM) preferred but not required
Experience:

Minimum of 3 years of experience in project management, clinical operations, or healthcare integration, preferably in oncology, research, or a related clinical setting
Experience facilitating the onboarding and training multidisciplinary clinical teams
Experience with the M365 suite including Excel and PowerPoint and experience with Smartsheet or other project management tools is preferred



Physical and Travel Requirements:

Required to travel up to 50% of the year, including travel to new clinic locations across the US
Physical Demands:

Sitting: Frequent, for administrative and training duties
Standing: Frequent, during training and setup activities
Bending: Occasional, for equipment setup or process implementation
Lifting: Ability to lift up to 25 pounds, occasionally, for handling supplies and equipment
Exposure to clinical environments, including areas where protective precautions are necessary



Best-in-Class Benefits and Perks
We value our employees&rsquo; time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:

Comprehensive health coverage: Medical, dental, and vision insurance provided
Robust retirement planning: 401(k) plan available with employer matching
Financial security: Life and disability insurance for added protection
Flexible financial options: Health savings and flexible spending accounts offered
Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided
Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.

More about The START Center for Cancer Research
Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including for 43 therapies that were approved by the FDA. START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. Learn more at STARTresearch.com.
Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.
We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Tue, 20 Jan 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Pharmacy Technician  - Grand Rapids, MI]]></title>
      <link>https://j.brt.mv/jb.do?reqGK=27769844&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>7dce9657-bd8b-4241-923a-c82330223814</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering access to cutting edge trials throughout the US and Europe. Today, with over 1,300 studies completed, and with research facilities in the United States and in Spain, Portugal, and Ireland, START&rsquo;s mission is to accelerate the development of new anticancer drugs that will improve the quality of life and survival for patients with cancer and lead to its eventual cure. To date, over 43 therapies conducted at START locations have obtained FDA/EMA approval. Incredibly, while Academic Medical Centers (AMCs) conduct 80% of cancer trials, such trials reach only 20% of the patient population &ndash; leaving the majority of patients who are treated in community practices and hospitals without access to a clinical trial when their care journey calls for one. START serves the many &ndash; by bringing cancer trials to physicians and their patients in community hospitals and practices when hope is needed most.
 
START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash; the most effective cancer drug in medical history.
We are hiring a Pharmacy Technician.  The role will assure safe, efficient, and cost-effective preparation of chemotherapy, biologic therapy, and supportive care medications for administration to patients following all applicable regulations. Also, this role will work collaboratively with Site Leaders and Pharmacists to maintain adequate and cost-effective inventory of drugs and supplies.
 Essential Responsibilities:

Mix and label chemotherapy, biologic therapy and supportive care medications. 
Perform proper procedures and documentation in inventory management systems during the fulfillment of the medication order. 
Prepare parenteral dosage forms utilizing aseptic techniques in accordance with departmental policies, standards set forth in current USP, state & federal regulations and GCP guidelines for investigational medications. 
Prepare and deliver medication ensuring proper storage location requirements are met based on the stability needs of the product. 
Perform routine weekly inventory and quality assurance tasks, including checking extemporaneously manufactured medications, commercially available medications, I.V. solutions and equipment for expiration dates, recalls, or signs of deterioration. 
Receive medication and supplies in accordance with inventory control and purchasing policies. Help to maintain all medication inventory levels within the predetermined stocking level, calling attention to needs for revision, or perpetual supply problems. 
Interact with study monitors by providing drug accountability reports and temperature storage logs. Facilitate monitor verification of inventory, training and other GCP documentation. 
Maintain and generate reports through the applicable computer programs.  
Other duties may be assigned at any time.

).Education & Experience

High School Diploma/GED. 
At least 2 years of experience preparing chemotherapy and biologic therapies. 
Current State registration as a pharmacy technician (CPhT). 

Best-in-Class Benefits and Perks
We value our employees&rsquo; time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:

Comprehensive health coverage: Medical, dental, and vision insurance provided
Robust retirement planning: 401(k) plan available with employer matching
Financial security: Life and disability insurance for added protection
Flexible financial options: Health savings and flexible spending accounts offered
Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided
Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.

More about The START Center for Cancer Research
Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including for 43 therapies that were approved by the FDA. START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. Learn more at STARTresearch.com.

Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Tue, 20 Jan 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Team Lead, Vivarium - San Antonio, TX]]></title>
      <link>https://j.brt.mv/jb.do?reqGK=27769264&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>4833CEA7-7B0F-011D-E063-0100007F9976</guid>
      <description><![CDATA[XenoSTART, the preclinical division of START is a translational research organization focused on creating relevant preclinical cancer models.  Our xenograft models represent each cancer type and disease stage and are established from patients at our domestic and international cancer centers. The XenoSTART Patient-Derived Xenograft (XPDX) platform includes over 2,500 models annotated with each donor patient&rsquo;s cancer treatment and outcome data and characterized using IHC, DNA/RNA sequencing, and relevant in vivo drug efficacy.
Our XPDX models are clinically annotated and include patient treatment history and outcome and are characterized through genomic profiling, histologic analysis, and in vivo drug sensitivity to relevant standards of care. These models may be utilized in the following manner:

In vivo PK/PD and efficacy studies
In vivo efficacy panel screens (indication or target focused)
In licensing of models for internal studies
Custom model development
Orthotopic and radiotherapy studies
Ex vivo and organoid studies

 We are hiring a Team Lead, Vivarium, who serves as a functional leader within the In Vivo Research team, coordinating daily activities and supporting process execution in line with study protocols. While this role does not have formal direct supervisory duties, the Team Lead is responsible for guiding team operations, facilitating communication between staff and management, and supporting new employee onboarding and training. This role involves supervising data collection from industry-sponsored and investigator-initiated studies, ensuring adherence to protocols and compliance with all regulatory and safety guidelines, and managing all procedures related to small animal handling, husbandry, surgery, drug preparation, and dosing. This position plays a key role in maintaining protocol compliance, animal welfare, and operational efficiency across the lab. 
 Essential Responsibilities:

Facilitate daily team huddles to communicate study updates and cross-functional information.
Serve as a key contributor in process improvement initiatives and ensure adherence to established standard work.
Monitor and track Key Performance Indicators (KPIs) as defined by leadership.
Act as a resource and technical mentor to new hires and team members requiring additional support.
Promote responsible use of resources and cost-effective practices.
Ensure all study-related documentation is current, accurate, and audit-ready.
Perform and oversee in vivo procedures, including small animal handling, dosing, surgery, tumor implantation, euthanasia, and sample collection/processing.
Administer agents according to protocol-specific dosing schedules and routes.
Collect and record data related to body weights, tumor measurements, and other endpoints using approved tools and software.
Ensure health and welfare of animals, maintaining compliance with AAALAC and IACUC standards.
Identify and escalate quality or compliance concerns to the appropriate supervisor or project manager.
Monitor Key Quality Indicators (KQIs) and ensure lab environments are maintained in a clean, safe, and OSHA-compliant state.
Participate in weekly cross-functional team meetings and provide study-related updates.
Assist in aligning daily study conduct with customer-defined deliverables and expectations.
Solicit feedback from internal stakeholders and escalate concerns as needed.
Support operations review meetings and share team performance insights as applicable.
Assist in the completion of study logs, inventory records, and compliance documentation.
Ensure all documentation is aligned with SOPs and regulatory expectations.
Other duties may be assigned at any time.

 Required Education and Experience:

Bachelor&rsquo;s degree in life sciences or related field.
3 years of related experience.
Proficiency in Microsoft Office applications.
Strong attention to detail and documentation practices.
Ability to work effectively in a fast-paced, team environment.

 Preferred Education and Experience:

 Bachelor&rsquo;s degree in life sciences or related field.
 Demonstrated experience in technical mentoring or functional leadership.
 Formal training in animal handling and in vivo research procedures.
 Familiarity with AAALAC, IACUC, and OSHA compliance.

 Best-in-Class Benefits and Perks
We value our employees&rsquo; time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:

Comprehensive health coverage: Medical, dental, and vision insurance provided
Robust retirement planning: 401(k) plan available with employer matching
Financial security: Life and disability insurance for added protection
Flexible financial options: Health savings and flexible spending accounts offered
Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided

Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.
 More about The START Center for Cancer Research
Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including for 43 therapies that were approved by the FDA. START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. Learn more at STARTresearch.com.
 Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.
 We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Mon, 12 Jan 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Oncology/Urology NP/PA - Myrtle Beach, SC]]></title>
      <link>https://j.brt.mv/jb.do?reqGK=27768232&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>461B09AD-E632-206C-E063-0100007FD2A9</guid>
      <description><![CDATA[The START Center for Cancer Research ("START") is the world's largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering access to cutting edge trials throughout the US and Europe. Learn more at STARTresearch.com.
Join Our Pioneering Team as an Advanced Practice Provider (APP) &ndash; Urology and Later Phase Clinical Research Program
Location: 823 82nd Pkwy, Suite B, Myrtle Beach, South Carolina 29572 - We offer willing to offer relocation assistance for the right fit!
The Advanced Practice Provider (APP) &ndash; Urology and Later Phase Clinical Research Program supports clinical care and protocol execution for urology-focused and later-phase oncology clinical trials. Operating as a sub-investigator under the supervision of the Principal Investigator (PI), the APP supports patient screening, study visits, and continuity of care while facilitating efficient clinic operations within a disease-focused research environment.
Schedule: Our clinic is open Monday through Friday from 8-5. We can be flexible with the schedule if a four day work week is preferred.
Essential Responsibilities:

Serve as a sub-investigator on assigned urology and later-phase clinical trials following completion of required training and delegation documentation.
Conduct protocol-required physical examinations and study visits for patients in screening, on treatment, and in follow-up as delegated by the Principal Investigator.
Prepare medical histories and clinical summaries in advance of new patient consults to support efficient PI evaluation.
Assist with patient screening activities, including chart review, protocol feasibility assessment, and coordination of required evaluations.
Support post-consent screening and ongoing study assessments in accordance with protocol requirements.
Assist with adverse event (AE) and serious adverse event (SAE) identification, documentation, and follow-up in collaboration with the Principal Investigator and research team.
Serve as a primary clinical contact for the research care team for routine patient management questions and escalate complex issues to the Principal Investigator.
Coordinate closely with nursing, clinical research coordinators, and ancillary services to support protocol adherence and patient-centered care.
Support disease-focused outreach, education, and multidisciplinary collaboration as requested.
Other duties may be assigned at any time.

Education & Experience:

Advanced practice degree (Nurse Practitioner or Physician Assistant) with current licensure in the state of South Carolina or ability to be licensed in the state of South Carolina.
Minimum of 3 to 5 years of experience in urology, oncology, or clinical research.

Preferred Education and Experience:

Master's degree or Doctoral degree in advanced practice nursing or physician assistant studies.
National certification as a Nurse Practitioner or Physician Assistant. Eligibility and willingness to serve as a sub-investigator on clinical trials.
Prior experience in urology clinical care or later-phase oncology clinical research.

Physical & Travel Requirements:

Travel: Limited travel may be required during training and onboarding.
Sitting: Must be able to sit for extended periods of time.
Standing: Must be able to stand for extended periods of time.
Bending: Must be able to reach overhead, at shoulder level, or bend to perform tasks.
Lifting: Must be able to lift up to 25 pounds.
Exposure: Works closely with physicians, research staff, and ancillary personnel in caring for and treating urology and oncology patients.

Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.]]></description>
      <pubDate>Tue, 16 Dec 2025 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[GU Medical Oncologist / Director, Clinical Research - Myrtle Beach, SC]]></title>
      <link>https://j.brt.mv/jb.do?reqGK=27761313&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>3C573CF7-824A-4B74-E063-0100007FE01C</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering access to cutting edge trials throughout the US and Europe. Today, with over 1,300 studies completed, and with research facilities in the United States and in Spain, Portugal, and Ireland, START&rsquo;s mission is to accelerate the development of new anticancer drugs that will improve the quality of life and survival for patients with cancer and lead to its eventual cure. To date, over 43 therapies conducted at START locations have obtained FDA/EMA approval. Incredibly, while Academic Medical Centers (AMCs) conduct 80% of cancer trials, such trials reach only 20% of the patient population &ndash; leaving the majority of patients who are treated in community practices and hospitals without access to a clinical trial when their care journey calls for one. START serves the many &ndash; by bringing cancer trials to physicians and their patients in community hospitals and practices when hope is needed most.
 
The Director, Clinical Research / Genitourinary (GU) Clinical Investigator is a physician-scientist with demonstrated clinical research team leadership skills responsible for the overall preparation, conduct, and management of GU Oncology clinical trials including Phase 1 studies. This role will manage the development and execution of clinical trial protocols, contribute to data analysis, and maintain strong communication and alignment with industry sponsors while maintaining compliance with all regulatory requirements and institutional policies. The Genitourinary (GU) Physician Investigator (PI) is a physician-scientist with demonstrated clinical research team leadership skills responsible for the overall preparation, conduct, and management of GU Oncology clinical trials including Phase 1 studies. This role will manage the development and execution of clinical trial protocols, contribute to data analysis, and maintain strong communication and alignment with industry sponsors while maintaining compliance with all regulatory requirements and institutional policies.

This role is based on site in Myrtle Beach, South Carolina.

Essential Responsibilities

Strong leadership skills to oversee early and late phase GU clinical trials by providing overarching medical direction and comprehensive medical reviews of protocols in conformance with the investigational plan and good clinical practice
Work collaboratively across healthcare provider disciplines with urologic oncologists, radiation oncologists, nuclear medicine radiologists, pathologists and medical oncology physicians
Provide medical and scientific feasibility of all new sponsor inquiries driving growth through strategic partnerships
Lead and manage a matrix team responsible for the conduct of GU oncology trials
Ensure the safety and well-being of all trial site participants are protected
Ensure data collected at the study site is credible and accurate
Ensure the ethical rights, integrity, and confidentiality of all participants at the trial site are protected
Develop professional working relationships with Sponsors and Clinical Research Organizations involved in study conduct
Provide expert guidance and support to clinical operations research staff and sponsor client
Lead continuous quality improvement efforts for clinical research services, integrating best practices and fostering a culture of research excellence and multidisciplinary collaboration
Develop and implement strategies to enhance patient recruitment and retention in clinical trials
Strong collaborative skills working with START Co-Investigator physicians and across the START Network.


Required Education and Experience:

M.D. or equivalent
Board Certified in Medical Oncology or Urology
Qualified for relevant US State Medical Licensing
Clinical trials experience with a strong interest in drug development and publications
Ability to critically analyze clinical scientific data and literature
Understanding of Good Clinical Practice (GCP) principles, safety and adverse event reporting, FDA regulations, and biomedical research ethics
Passion for providing excellence of clinical care and for working in a collaborative / team-oriented environment
Strong leadership skills with entrepreneurial mindset encompassing an aggressive approach to growth and expansion


Preferred Education and Experience:

Previous experience with industry sponsored clinical trials
Excellent communication skills, with experience in publishing and presenting at scientific meetings
Translational research experience and familiarity with early and late-stage clinical trials

Best-in-Class Benefits and Perks
We value our employees&rsquo; time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:

Comprehensive health coverage: Medical, dental, and vision insurance options provided
Robust retirement planning: 401(k) plan available with employer matching
Financial security: Company-paid life and disability insurance for added protection
Flexible financial options: Health savings and flexible spending accounts offered
Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided
Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.


More about The START Center for Cancer Research
Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including for 43 therapies that were approved by the FDA. START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. Learn more at STARTresearch.com.

Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Thu, 14 Aug 2025 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Medical Oncologist / Director, Clinical Research - East Brunswick, NJ]]></title>
      <link>https://j.brt.mv/jb.do?reqGK=27761312&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>3C573CF7-8240-4B74-E063-0100007FE01C</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering access to cutting edge trials throughout the US and Europe. Today, with over 1,300 studies completed, and with research facilities in the United States and in Spain, Portugal, and Ireland, START&rsquo;s mission is to accelerate the development of new anticancer drugs that will improve the quality of life and survival for patients with cancer and lead to its eventual cure. To date, over 43 therapies conducted at START locations have obtained FDA/EMA approval. Incredibly, while Academic Medical Centers (AMCs) conduct 80% of cancer trials, such trials reach only 20% of the patient population &ndash; leaving the majority of patients who are treated in community practices and hospitals without access to a clinical trial when their care journey calls for one. START serves the many &ndash; by bringing cancer trials to physicians and their patients in community hospitals and practices when hope is needed most.
 
START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash; the most effective cancer drug in medical history.

We are seeking a Director, Clinical Research / Clinical Investigator. The Clinical Principal Investigator (PI) is a physician-scientist responsible for the overall preparation, conduct, and management of sponsored projects, ensuring compliance with all regulatory requirements and institutional policies. This role will manage the development and execution of clinical trial protocols, contribute to data analysis, and maintain strong communication and alignment with sponsors.

This role is based on site in East Brunswick, New Jersey.

Essential Responsibilities

Manage early phase clinical trials by providing overarching medical direction and comprehensive medical reviews of protocols in conformance with the investigational plan and good clinical practice.
Provide medical and scientific feasibility of all new sponsor inquiries driving growth through strategic partnerships.
Lead and manage a matrix team of responsible for responsible for the conduct of early phase oncology trials.
Ensure the safety and well-being of all participants in the study at the trial site are protected.
Ensure data collected at the study site is credible and accurate.
Ensure the rights, integrity, and confidentiality of all participants in the trial at the site are protected.
Develop close personal working relationships with Sponsors and Clinical Research Organizations involved in study conduct.
Provide expert guidance and support to clinical operations research staff and sponsor client.
Lead continuous quality improvement efforts for clinical research services, integrating best practices and fostering a culture of research excellence.
Develop and implement strategies to enhance patient recruitment and retention in clinical trials.


Required Education and Experience:

M.D. or equivalent.
Board Certified in Hematology and/or Medical Oncology.
Clinical trials experience with a strong interest in drug development.
Ability to critically analyze clinical scientific data and literature.
Understanding of GCP principles, safety and adverse event reporting, FDA regulations, and biomedical research ethics.
A passion for providing excellent clinical care and for working in a collaborative / team-oriented environment.


Preferred Education and Experience:

Previous experience with industry sponsored clinical trials.
Excellent communication skills, with experience in publishing and presenting at scientific meetings.
Translational research experience and familiarity with pharmacokinetics and pharmacodynamics.


Best-in-Class Benefits and Perks
We value our employees&rsquo; time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:

Comprehensive health coverage: Medical, dental, and vision insurance options provided
Robust retirement planning: 401(k) plan available with employer matching
Financial security: Company-paid life and disability insurance for added protection
Flexible financial options: Health savings and flexible spending accounts offered
Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided
Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.


More about The START Center for Cancer Research
Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including for 43 therapies that were approved by the FDA. START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. Learn more at STARTresearch.com.

Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Thu, 14 Aug 2025 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Director of Business Development (Remote) - San Antonio, TX]]></title>
      <link>https://j.brt.mv/jb.do?reqGK=27758101&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>3844D628-E734-3635-E063-0100007F1605</guid>
      <description><![CDATA[XenoSTART, the preclinical division of START is a translational research organization focused on creating relevant preclinical cancer models.  Our xenograft models represent each cancer type and disease stage and are established from patients at our domestic and international cancer centers. The XenoSTART Patient-Derived Xenograft (XPDX) platform includes over 2,500 models annotated with each donor patient&rsquo;s cancer treatment and outcome data and characterized using IHC, DNA/RNA sequencing, and relevant in vivo drug efficacy.

Our XPDX models are clinically annotated and include patient treatment history and outcome and are characterized through genomic profiling, histologic analysis, and in vivo drug sensitivity to relevant standards of care. These models may be utilized in the following manner:

In vivo PK/PD and efficacy studies
In vivo efficacy panel screens (indication or target focused)
In licensing of models for internal studies
Custom model development
Orthotopic and radiotherapy studies
Ex vivo and organoid studies

We are hiring a dynamic and results-driven Director of Business Development to join our team at XenoSTART. As a key player in our sales force, you will be responsible for understanding XenoSTART's unique selling proposition and translating it into effective solutions tailored to each customer's needs. This role requires a keen understanding of the Pre-Clinical sales process along with the ability to manage and exceed performance objectives in an assigned territory or named accounts. 
This is a remote role. The annual base salary for this role is $140,00 - $150,000 + Commission. However, base pay may vary depending on multiple individualized factors including market location, job-related knowledge, skills, and experience. 

Essential Responsibilities

Meet and or exceed assigned sales and revenue targets.
Expand our share of studies at existing clients.
Acquire new clients in partnership with the demand generation team.
Build client commitment at each stage of the sales process.
Participate in the contract review process to get client consensus, as needed.
Develop and manage comprehensive account development plans (Miller Heiman preferred); track progress against key account development milestones; report progress in regularly scheduled account review sessions.
Identify and build relationships with key decision makers internally and externally.
Manage and record all client interaction through Hubspot. This includes accurate entry and upkeep of details for Accounts, Contacts, Calls, Tasks, Events, Opportunities and Client Referrals for a comprehensive CRM profile of each client.
Work collaboratively with Finance to provide and maintain a regular forecast to ensure the business has clear visibility of future opportunities.
Other duties may be assigned at any time.

Education & Experience


5+ years of sales experience within a CRO, with demonstrated success selling PDX models and/or leveraging a strong scientific background in oncology.

Bachelor&rsquo;s degree required.
Exhibit a high degree of interpersonal and persuasive communication skills.
Demonstrated success in building collaborative relationships within an organization.
Demonstrated success with goal attainment in dynamic environment. 
Demonstrated knowledge of competition and developed persuasive strategies to win competitive opportunities.
Strong analytical skills and the ability to draw conclusions and observations from Market trends.
Strong presentation skills.
Focused, with demonstrated work ethic, personal motivation, and enthusiasm; takes personal pride in accomplishment.

Preferred Education and Experience:

Bachelor&rsquo;s degree in the Sciences.
Prior work experience supporting and working for a company with a focus on Pre-Clinical Oncology studies or Contract Research Organization (CRO), strongly preferred. 

Physical and Travel Requirements:  

Travel Expectations: Travel up to 40%.
Travel and meet clients as necessary, including Europe when necessary.
Travel to clients and trade shows, workshops, etc. as necessary.
Mobility: traveling often involves moving between different locations. Must be able to handle demands of navigating airports, public transportation, and various work environments.
Sitting: Ability to remain seated for extended periods of time.

Best-in-Class Benefits and Perks
We value our employees&rsquo; time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:

Comprehensive health coverage: Medical, dental, and vision insurance provided
Robust retirement planning: 401(k) plan available with employer matching
Financial security: Life and disability insurance for added protection
Flexible financial options: Health savings and flexible spending accounts offered
Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided
Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.


More about The START Center for Cancer Research
Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including for 43 therapies that were approved by the FDA. START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. Learn more at STARTresearch.com.

Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Mon, 23 Jun 2025 00:00:00 EDT</pubDate>
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