The Clinical Research Coordinator (CRC) is responsible for managing and coordinating clinical trials in compliance with regulatory guidelines, study protocols, and institutional policies. The role involves patient recruitment, data collection, documentation, and ensuring smooth execution of research activities.
Key Responsibilities:
- Coordinate and manage clinical research studies as per approved protocols
- Screen, recruit, and enroll eligible patients for clinical trials
- Obtain informed consent from study participants
- Maintain accurate and timely documentation of study-related activities
- Collect, record, and report clinical data in case report forms (CRFs)
- Ensure compliance with ICH-GCP, regulatory, and institutional guidelines
- Liaise with investigators, sponsors, ethics committees, and other stakeholders
- Schedule and coordinate patient visits, follow-ups, and procedures
- Monitor patient safety and report adverse events as per protocol
Pay: ₹20,000.00 - ₹22,000.00 per month
Benefits:
- Health insurance
- Provident Fund
Work Location: In person
