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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 in office 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 Compensation: 275,000.00 - 330,000.00 per year Benefits: - Health insurance - Paid sick time - Work from home Work Location: In person .