Study Coordinator

UNC; Chapel Hill (NC); Sur place; USD 65 000 - 90 000; Plein temps

Résumé du poste

UNC/LCCC Clinical Trials Office seeks a Clinical Trials Coordinator to advance oncology research and improve patient outcomes by ensuring trials meet federal regulations and Good Clinical Practice.

The role independently manages multiple complex trials through activation, implementation, and closure under supervision, coordinating visits, documenting procedures, and supporting patient safety and regulatory compliance across UNC clinics.

Responsabilités

• Recruitment, consent, and enrollment of study participants.
• Coordinate study visits across clinic settings.
• Document procedures and visits; facilitate sample collection and data entry.
• Collaborate with research teams to ensure regulatory compliance and patient safety.

Description du poste

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.