Study Coordinator

UNC-Chapel Hill • Chapel Hill, NC

19h

About The Position

This position advances cancer research and improves patient outcomes by facilitating oncology clinical trials in compliance with federal regulations, Good Clinical Practice, and institutional policies. 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 is integral to the mission of the UNC / LCCC Clinical Trials Office. It helps maintain research quality and institutional integrity while supporting discoveries that shape the future of cancer care.

Requirements

• Ensure clinical trials comply with federal regulations, Good Clinical Practice, and institutional policies.

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.
• Independently manage multiple complex trials through activation, implementation, and closure.

What This Job Offers

• Job Type: Full-time
• Education Level: No Education Listed