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Site Development Specialist,(Remote,Travel)

Job Title
Site Development Specialist,(Remote,Travel)
Job ID
27691980
Location
Austin,  TX 78738
Other Location
Description

JOB SUMMARY  

Position requires approximately 50% travel

The Site Development Specialist (SDS) plays a key role in ensuring that Elligo PoweredBy® sites are qualified to conduct and execute the clinical studies effectively and efficiently. Is the primary point of contact for new Elligo Traditional sites. The SDS provides Study Management support to all sites or practices where trial support is needed.  

Responsibilities may include, but are not limited to: 

  • Provides site set up expertise to ensure new Elligo sites are in a position to qualify for and conduct clinical trials as quickly as possible after identification 

  • Evaluates site equipment needs and works with others at Elligo to ensure the appropriate research infrastructure is in place 

  • Assists with new investigator and site/practice staff training  

  • When applicable, serves as the study management point of contact for feasibility, PSVs, etc after practice handover and before a study manager/coordinator has been identified 

  • Assists with training and onboarding (where appropriate) of new study staff (SM, SC) at sites/practices 

  • Assists with the interviews for new SC, SM staff 

  • Facilitates pre-study, site qualification, study initiation, monitoring visits and study close out activities for PoweredBy® sites 

  • Verifies the SDS playbook is followed for site set up, relationships and interactions 

  • Works with site personnel and Elligo project leads to monitor and assure Elligo/PoweredBy® services are delivered on time and with accuracy and completeness 

  • Manages documentation for all Elligo/PoweredBy® sites including training & development, SOPs 

  • Provides oversight of new SC, SM hires for up to 6 months to ensure they are competent in their role 

  • Works to cultivate productive relationships between site/practice and study personnel which will result in ongoing cooperation related to the coordination of research procedures, study visits and follow-up 

  • Maintains confidentiality, prioritizes and manages work effectively and provides exceptional customer service internally and externally 

  • Demonstrates knowledge of the Company’s clinical research studies  

  • Works cross functionally with other departments/groups  

  • Performs other duties and responsibilities as required 

QUALIFICATION AND EDUCATION REQUIREMENTS  

 

  • BS/BA in Life Science or related discipline. CCRC/CCRP certification preferred. 

  • Requires a minimum 4 yrs experience coordinating clinical research studies at a healthcare site (including Industry-sponsored research studies) or equivalent experience such as that of a Clinical Research Associate  

  • Demonstrated ability in positive relationship building, with strong verbal and written skills required  

  • Previous supervisory experience preferred 

  • 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)  

  • Strong organization/prioritization skills for the management of multiple concurrent projects  

 

The primary skill sets needed to be successful in this position include: project and personnel management, logical thinking, prioritization proficiencies, a “can-do” attitude, interpersonal and team building skills, along with the ability to adapt quickly to changing business conditions 

 

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 travel (50% or more) 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 in-depth 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!”

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Business Analyst, Business Development

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