A Clinical Research Coordinator (CRC) manages the daily operations of clinical trials, ensuring participant safety and protocol compliance. They recruit/screen patients, obtain informed consent, collect data, manage study documents, and report adverse events. They act as the primary liaison between investigators, sponsors, and participants.
Key Responsibilities
- Coordinate day-to-day clinical trial operations at the site
- Screen, recruit, and enroll study participants
- Obtain and document informed consent
- Schedule subject visits and follow-ups
- Collect, record, and maintain accurate study data
- Maintain regulatory documents and study files
- Ensure compliance with study protocols and GCP guidelines
- Report adverse events and safety information
- Prepare for monitoring visits, audits, and inspections
- Liaise with investigators, sponsors, and monitors
Required Qualifications
- Bachelor’s or Master’s degree in Life Sciences / Pharmacy / Nursing / Medical field
Job Types: Full-time, Permanent, Fresher
Pay: ₹18,000.00 - ₹25,000.00 per month
Benefits:
- Health insurance
- Paid sick time
Work Location: In person
