Temporary Study Coordinator
Listed on 2026-02-09
-
Healthcare
Overview
Be a Tar Heel! A global higher education leader in innovative teaching, research and public service, the University of North Carolina at Chapel Hill consistently ranks as one of the nation’s top public universities. Known for its beautiful campus, world-class medical care, commitment to the arts and top athletic programs, Carolina is an ideal place to teach, work and learn. One of the best college towns and best places to live in the United States, Chapel Hill has diverse social, cultural, recreation and professional opportunities that span the campus and community.
University employees can choose from a wide range of professional training opportunities for career growth, skill development and lifelong learning and enjoy exclusive perks that include numerous retail and restaurant discounts, savings on local child care centers and special rates for performing arts events.
- Department: LCCC - Clinical Trials - 426806
- Career Area: Research Professionals
- Posting Open Date: 02/02/2026
- Final date to receive applications: 02/05/2026
- Position Type: Temporary Staff (SHRA)
- Position Title: Temporary Study Coordinator
- Position Number:
- Vacancy : S026820
- Full-time/Part-time: Part-Time Temporary
- Hours Per Week: 10
- Work Schedule: Monday – Friday, 8:30 AM – 5:00 PM
- Position Location: North Carolina, US
- Hiring Range: $34.84 - $37.29 per hour
- Proposed
Start Date:
02/09/2026 - Estimated Duration Of Appointment: 4 months or less
Reporting to the Clinical Operations Manager, this part-time, temporary study coordinator position plays a pivotal role in advancing cancer research and improving patient outcomes by facilitating the conduct of oncology clinical trials in compliance with federal regulations, Good Clinical Practice, and institutional policies. This position independently manages multiple complex trials throughout their life cycle, including activation, implementation, and closure, under the direction of a Clinical Operations Manager.
Key Responsibilities- Being a resource for assigned studies
- Assist with study training and education
- Data entry
- Map out study processes
- Other duties as assigned
This position is integral to the mission of the UNC/LCCC Clinical Trials Office, maintaining research quality and safeguarding institutional integrity, and driving discoveries that shape the future of cancer care.
Minimum Education And Experience RequirementsBachelor’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.
Management Preferences- Previous experience with therapeutic clinical research involving drugs and/or devices
- Experience with direct patient contact in the hospital/clinic setting
- Experience or familiarity with medical terminology
- Demonstrated ability to operate at a high degree of independence
- Demonstrated ability to coordinate studies of high complexity
Campus Security Authority Responsibilities Not Applicable.
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