- Assist in monitoring clinical trial sites and study activities.
- Ensure compliance with study protocols, GCP (Good Clinical Practice), and regulatory requirements.
- Review and maintain trial documentation and case report forms (CRFs).
- Coordinate with investigators, site staff, and sponsors.
- Support site initiation, monitoring visits, and close-out activities.
- Track patient recruitment and study progress.
- Maintain accurate records and prepare study reports.
- Assist in resolving data queries and discrepancies.
- Ensure proper handling and storage of study materials.
Pay: ₹17,500.00 - ₹26,000.65 per month
Benefits:
- Cell phone reimbursement
- Flexible schedule
- Paid sick time
Work Location: In person
