A CRA ensures that clinical trials are conducted ethically, safely, and in strict compliance with the study protocol and regulatory standards like Good Clinical Practice (GCP).
- Key Responsibilities:
- Site Monitoring: Conducting on-site or remote visits to verify that trial data matches original medical records (Source Data Verification).
- Compliance: Ensuring the rights, safety, and well-being of trial participants are protected and that all regulatory approvals are in place.
- Training & Liaison: Briefing site staff (doctors and coordinators) on trial procedures and acting as the primary point of contact for the sponsor.
- Documentation: Preparing detailed monitoring reports and managing essential study files to ensure they are "audit-ready".
Job Types: Full-time, Permanent, Fresher
Pay: ₹275,000.00 - ₹330,000.00 per year
Benefits:
- Health insurance
- Paid sick time
- Work from home
Work Location: In person
