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UO
University of North Carolina at Chapel Hill
Associate Clinical Research Coordinator
Entry-Level JobVerifiedNo experience needed
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What they do
A Clinical Research Coordinator directs clinical research and development projects for companies, and coordinates testing and quality control.
$111,747 / year median in North Carolina
+12% projected growth
Job Description
Posting Information Department OBGYN-Urogynecology-412460 Career Area Research Professionals Is this an internal only recruitment? No Posting Open Date 08/18/2026 Application Deadline 09/01/2026 Position Type Permanent Staff (SHRA) Position Title Soc/Clin Research Assistant
- Advanced Salary Grade Equivalent
NC10 / GN10
Working Title Associate Clinical Research Coordinator Position Number 20069245 VacancyID P021300
Full-time/Part-time Permanent/Time-Limited Full-Time Time-Limited If time-limited, estimated duration of appointment 2 years Hours per week 40 Work Schedule Monday- Friday, 7:30 AM
- 4:30 PM Work Location Raleigh, NC Position Location North Carolina, US Hiring Range $55,885
- $65,000 Pay Band Information To learn more about the pay band for this branch and role, please see the Career Banding rates spreadsheet .
Patient care:
We promote health and provide superb clinical care while maintaining our strong tradition of reaching underserved populations and reducing health disparities across North Carolina and beyond.Education:
We prepare tomorrow's healthcare professionals and biomedical researchers from all backgrounds by facilitating learning within innovative and integrated curricula and team-oriented interprofessional education to ensure a highly skilled workforce.Research:
We develop and support a rich array of outstanding health sciences research programs, centers and resources. We provide infrastructure and opportunities for collaboration among disciplines throughout and beyond our university to support outstanding research. We foster programs in the areas of basic, translational, mechanistic and population research. Position Summary This position will serve as an Associate Clinical Research Coordinator within the Department of Obstetrics and Gynecology, Division of Urogynecology. The Associate Clinical Research Coordinator is responsible for the execution of clinical research protocols, including leading efforts in gathering, compiling, and reporting data for a variety of research studies. This is a time-limited position with an estimated duration of 2 years, with potential for an extension. This is an in-person position at the UNC Urogynecology office in Raleigh. Ability to work in Raleigh, with potential travel to other UNC Health campuses for study-related activities, is a requirement of this position. This position is responsible for helping to support divisional research staff with the administration and management of multiple new and existing research projects in the Division of Urogynecology, which is located at the UNC Urogynecology office in Raleigh. The Associate Clinical Research Coordinator will be responsible for assisting in recruitment, scheduling, visit conduct, data collection, data entry, and monitoring. This position will be familiar with IRB process and with clinical research situations. The position will communicate clearly and effectively with primary investigators (PI) and be familiar with medical terminology. The position will adhere to standards of proper study conduct in compliance with the FDA Code of Federal Regulations and Good Clinical Practice. The position will inform and help the PIs with issues that arise during study execution, aid with preparation for monitoring or audits, and help with the collection of study results. Minimum Education and Experience Requirements Bachelor's degree; or equivalent combination of training and experience. All degrees must be received from appropriately accredited institutions. Management Preferences Knowledge of research principles such as GCP and FDA regulations. Prior experience or knowledge relating to the field of urogynecology. Experience with industry-sponsored, federally funded, PI initiated, or pilot studies. Strong written and verbal communication skills in order to work and communicate with diverse populations effectively and professionally. Proficient with Microsoft Outlook, Excel, and Word. Required Licenses/Certifications Special Physical/Mental Requirements Availability for variable work schedules. Ability to work in Raleigh, with potential travel to other UNC Health campuses for study-related activities. Campus Security Authority Responsibilities Not Applicable. Position/Schedule RequirementsBenefits
- Paid Time Off (PTO)
- Dental Insurance
- Other Retirement and Savings