- Monitor and manage clinical trial sites and study activities.
- Ensure compliance with study protocols, SOPs, ICH-GCP, and regulatory requirements.
- Conduct site initiation, monitoring, and close-out visits.
- Verify source data and ensure accurate data entry and documentation.
- Coordinate with investigators, sponsors, ethics committees, and study staff.
- Maintain Trial Master File (TMF) and essential clinical documents.
- Report protocol deviations, adverse events, and safety issues.
- Assist in patient recruitment and retention strategies.
- Prepare monitoring reports and study progress updates.
- Ensure timely resolution of site-related queries and issues.
Pay: ₹25,000.00 - ₹40,000.00 per month
Benefits:
Work Location: In person
