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Clinical Research Study Coordinator, Laredo, TX (Texas applicants willing to relocate)

Job Title
Clinical Research Study Coordinator, Laredo, TX (Texas applicants willing to relocate)
Job ID
27603152
Location
Laredo,  TX 78045
Other Location
Description

JOB SUMMARY

*** Relocation Assistance may be discussed for this position***

This individual will play a key role in assisting in the conduct of clinical trial activities, in

accordance with all applicable regulations governing the conduct of clinical trials. The

primary skills include logical thinking, ability to prioritize, “can-do” attitude, the ability to

adapt quickly to changing business conditions, strong interpersonal and team building

skills.

 

The employee, working closely with study team members under the direct supervision

of a Study Manager, will support other study team members in order to achieve study

objectives and corporate goals, including:

  • Develop strong working relationships and maintain effective communication with study team members.
  • Become the point of contact for the clinic as well as the sponsor for clinic related
  • activities.
  • Manage multiple concurrent trials
  • Completes all protocol related training
  • Perform patient/research participant scheduling
  • Collect patient/research participant history
  • Collects and maintains source documentation
  • Performs data entry and query resolution
  • Support the collection and review of required essential study documents and reports. Order supportive study supplies (e.g., contracts, IXRS, lab kits, nonclinical supply materials, imaging and laboratory handling manuals, etc.).
  • Adhere to an IRB approved protocol
  • Assist in the informed consent process of research subjects.
  • Support the safety of research subjects, report adverse events.
  • Coordinate protocol related research procedures, study visits, and follow-up
  • Assist with the screening, recruiting and enrollment of research subjects.
  • Facilitate pre-study, site qualification, study initiation, monitoring visits, and study
  • close out activities
  • Collect, process and ship laboratory specimens
  • Comply with Elligo, Clinic, and Sponsor policies, standard operating procedures
  • (SOPs) and guidelines.

 

QUALIFICATION AND EDUCATION REQUIREMENTS

 

  • Associates Degree or BS/BA in Life Science or related discipline
  • Previous nursing experience in a clinical setting a plus
  • At least one year of experience in coordinating clinical trials
  • Prior training in GCP requirements
  • Strong interpersonal skills with attention to detail a must.
  • Demonstrated proficiency with word processing, spreadsheet, database, and
  • presentation software (MS Office skills such as Outlook, Word, Excel,
  • PowerPoint, SharePoint) and with clinical trial master filing systems.

 

WORKING CONDITIONS

 

This job operates in a professional office environment. This role routinely uses standard

office equipment such as computers, phones, and photocopiers.

Some flexibility in hours is allowed, but the employee must be available during the “core”

work hours of 9:30 a.m. to 3:30 p.m. and must work 37.5 hours each week to maintain

full-time status. Occasional evening and weekend work may be required as job duties

demand. Regular local and regional travel is required for this position.

 

The above statements are intended to describe the general nature and level of work being

performed by individuals assigned to this position. They are not intended to be construed

as an exhaustive list of responsibilities, duties, and skills required of personnel. More indepth

information can be found in SOP's, working guidelines, policies, etc.

 

Elligo is committed to the principle of equal employment opportunity for all employees

and to providing employees with a work environment free of discrimination and

harassment. All employment decisions at Elligo are based on business needs, job

requirements and individual qualifications, without regard to race, color, religion or belief,

national, social or ethnic origin, sex (including pregnancy), age, physical, mental or

sensory disability, HIV Status, sexual orientation, gender identity and/or expression,

marital, civil union or domestic partnership status, past or present military service, family

medical history or genetic information, family or parental status, or any other status

protected by the laws or regulations in the locations where we operate. Elligo will not

tolerate discrimination or harassment based on any of these characteristics. In addition,

Elligo will provide reasonable accommodations for qualified individuals with disabilities.

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“I am super passionate about what we are doing at Elligo and feel so fortunate to be a part of it! I haven’t been this excited about a job in years!”

Janet L.
Client Relations Specialist

“Having been involved in clinical research for over 10 years, I have found the Elligo model to be truly innovative. From top to bottom, the Elligo team is made up of professionals who use their experience and knowledge to positively affect the need to bring healthcare and clinical research together.”

James C.
Director, Clinical Operations

“Elligo is at the forefront of innovation in the clinical research industry. It’s rewarding to work among such highly motivated and distinguished leaders and visionaries. I start work each day feeling valued and end each day excited to be part of Elligo’s influence on changing the clinical research industry.”

Julie M.
Study Manager, Clinical Operations

“Working at Elligo has been a very unique experience. I love the fact that I’m surrounded by colleagues who help me learn something new every day. I value their experience and genuinely enjoy the work and projects we are involved with. I love coming to work every day!”

Alexandra B.
Business Analyst, Business Development

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