A Clinical Research Coordinator (CRC) is a clinical research professional responsible for conducting clinical trials according to regulatory and protocol guidelines. The CRC works closely with and under the supervision of a Principal Investigator (PI) to manage patient recruitment, data collection, and study administration. CRCs are often the primary liaison for the clinical research site. They will felp facilitate day-to-day activities and provide support throughout the clinical trial.
Primary Responsibilities:
- Patient Recruitment and Enrollment
- Data Collection and Documentation
- Protocol Compliance and Implementation
- Study Administration and Coordination
- Quality Assurance and Audits
- Patient Care and Support