Study Coordinator
About The Position
This position facilitates oncology clinical trials in compliance with federal regulations, Good Clinical Practice, and institutional policies to advance cancer research and improve patient outcomes. The Study Coordinator independently manages multiple complex trials throughout their life cycle, including activation, implementation, and closure, under the direction of a Clinical Operations Manager. The role supports the mission of the UNC / LCCC Clinical Trials Office by maintaining research quality, safeguarding institutional integrity, and driving discoveries that shape the future of cancer care.
Responsibilities
- Recruit, consent, and enroll study participants.
- Coordinate study visits across various clinic settings.
- Document procedures and visits, facilitate sample collection, and enter data.
- Collaborate with research teams to ensure regulatory compliance and patient safety.
- Manage multiple complex trials through activation, implementation, and closure.
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What This Job Offers
Job Type
Full-time
Education Level
No Education Listed
