Regulatory Clinical Research Coordinator - Temp
Listed on 2026-01-12
-
Healthcare
Clinical Research
Position Title
Regulatory Clinical Research Coordinator - Temp
DepartmentOrthopaedics - 414601
Career AreaResearch Professionals
Posting Open Date01/05/2026
Final date to receive applications01/11/2026
Position TypeTemporary Staff (SHRA)
Position NumberVacancyS026664
Full-time/Part-timeFull-Time Temporary
Hours per week40
Work ScheduleTo be determined by supervisor and selected candidate.
Position LocationNorth Carolina, US
Hiring Range$25.00 - $27.00 per hour
Estimated Duration of Appointment6 months not to exceed 11 months
Primary Purpose of Organizational UnitOur mission is to improve the health and well-being of North Carolinians and others whom we serve. We accomplish this by providing leadership and excellence in the interrelated areas of patient care, education and research.
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.
The Regulatory Clinical Research Coordinator position is to support our growing Orthopaedic research program including clinical research coordinators (CRCs) and principal investigators (PIs) with clinical research start-up and regulatory activities. This role is responsible for maintaining regulatory compliance across multiple protocols while supporting research professionals and faculty to ensure studies are conducted efficiently, accurately and in accordance with institutional policies, federal regulations, and Good Clinical Practice (GCP).
The key responsibilities include preparing, submitting and maintaining regulatory documents for IRB submissions, including initial submissions, amendments, continuing reviews and reportable events, maintaining complete and audit‑ready regulatory binders (electronic and/or paper), assisting with investigator documentation (e.g., CVs, licenses, CITI/GCP training records, delegation of authority logs), and supporting study start‑up activities including regulatory approvals and site readiness and feasibility.
Minimum Education and Experience RequirementsBachelor’s degree; or equivalent combination of training and experience. All degrees must be received from appropriately accredited institutions.
Required Qualifications , Competencies, and ExperienceComfortable engaging patients via phone conversations.
Preferred Qualifications , Competencies, and ExperienceRecruitment experience.
Campus Security Authority ResponsibilitiesNot Applicable.
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