Oncology Clinical Trials Study Coordinator

The University of North Carolina at Chapel Hill; Chapel Hill (NC); On-site; USD 64,000 - 75,000; Full time

Job summary

The University of North Carolina at Chapel Hill is seeking a Study Coordinator to drive oncology clinical trials, ensuring adherence to ICH-GCP and institutional policies. You will independently manage multiple trials from activation to closure under supervision, coordinating visits, consent, data collection, and safety oversight.

The role requires a Bachelor’s degree with related experience, strong regulatory knowledge, and excellent communication.

Qualifications

• Bachelor’s degree in a related field with minimum one year of related experience.
• Experience coordinating oncology clinical trials preferred.
• Familiarity with regulatory requirements and clinical protocols.
• Strong data entry and documentation accuracy.

Responsibilities

• Recruitment, consent, and enrollment of study participants
• Coordination of study visits across clinic settings
• Documentation of procedures and visits and data entry

Skills

Clinical research coordination

Regulatory compliance

Data abstraction & documentation

Communication skills

Education

Bachelor's degree in related field

Job description

The University of North Carolina at Chapel Hill is seeking a Study Coordinator to drive oncology clinical trials, ensuring adherence to ICH-GCP and institutional policies. You will independently manage multiple trials from activation to closure under supervision, coordinating visits, consent, data collection, and safety oversight.

The role requires a Bachelor’s degree with related experience, strong regulatory knowledge, and excellent communication.