Senior Study Coordinator

Job description

Position Type:

Permanent Staff (SHRA)

Is this an internal only recruitment?:


Position Title:

Soc/Clin Research Specialist - Journey

Working Title:

Senior Study Coordinator

Position Number:


Vacancy ID:


Budgeted Hiring Range:

$53,772 - $58,000

Pay Band Information:

To learn more about the pay band for this branch and role, please see the Career Banding rates spreadsheet.

Salary Grade Equivalent:


Full-time/Part-time Permanent/Time-Limited:

Full-Time Time-Limited

If time-limited, estimated duration of appointment:

3 years

Hours per week:


Work Schedule:

Monday – Friday 8:00 am to 5:00 pm

Department Name and Number:


Date First Posted:


Closing Date:


Position Location:

Chapel Hill, NC

Position Posting Category:

Research Professionals

Department Description:

The UNC Diabetes Care Center provides coordinated, comprehensive health care to patients with diabetes mellitus in a cost-effective manner. Additionally, the Center is a resource for the education of physician, allied health professionals, and lay people. Finally, and most pertinent to this position, the Center’s Clinical Trials Unit is involved in pursuing research aimed at developing improved diagnosis, treatment, and prevention of diabetes and obesity. The Center maintains an administrative office in Burnett- Womack, and a clinic/clinical trials unit at Meadowmont, where this position is located.

Equal Opportunity Employer:

The University of North Carolina at Chapel Hill is an equal opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to age, color, disability, gender, gender expression, gender identity, genetic information, race, national origin, religion, sex, sexual orientation, or status as a protected veteran.

Position Description:

The primary purpose of this position is to function as a Senior Study Coordinator, carrying out all aspects of clinical trials in diabetes and/or weight loss. This includes managing IRB submissions, regulatory and start-up work, study patient visits, data collection and quality assurance, as well as involvement in training new staff and supervising research associates.

Minimum Education and Experience Requirements:

Bachelor’s degree in a discipline related to the field assigned and one year of related training or experience; or equivalent combination of training and experience. All degrees must be received from appropriately accredited institutions.

Essential Skills, Knowledge and Abilities:

Must possess experience working with human clinical trials. Must have experience with IRB submissions. Must have experience with clinical trials data collection and entry.

Preferred Qualifications:

Preferred candidate would be a Registered Dietician.

Stimulus/ARRA Funded:





Diversity Profile: University



View more

Learn more on Inside Higher Ed's College Page for University

Arrow pointing right
Job No:
Posted: 4/7/2021
Application Due: 4/14/2021
Work Type: Full Time