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

📌 Clinical Research Associate (India)
🏢 Klinscience Healthcare
📍 India