- Assist in site selection, initiation, monitoring, and close-out visits.
- Ensure that clinical trials are conducted in accordance with protocols, SOPs, GCP, and regulatory requirements.
- Verify the accuracy and completeness of case report forms (CRFs) and source documents.
- Maintain essential documents in the Trial Master File (TMF).
- Assist in resolving data queries and discrepancies with the site staff.
- Support investigators and site staff in trial-related activities.
- Participate in project team meetings and training sessions.
- Prepare visit reports and follow-up letters.
- Maintain regular communication with study sites to ensure compliance and timely data entry.
Job Types: Full-time, Permanent, Fresher
Pay: ₹20,778.01 - ₹36,570.20 per month
Benefits:
- Health insurance
- Paid sick time
- Provident Fund
Work Location: In person
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