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UNC

Study Coordinator

UNC, Chapel Hill, North Carolina, United States, 27517

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This 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 include:

Recruitment, consent, and enrollment of study participants

Coordination of study visits across various clinic settings

Documentation of procedures and visits, facilitation of sample collection, and data entry

Collaboration with research teams to ensure regulatory compliance and patient safety

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.

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