Key Responsibilities
- Collect and process reports of adverse drug reactions from patients, doctors, and clinical trials
- Enter and maintain safety data in pharmacovigilance databases
- Assist in case processing and follow-ups for missing information
- Support preparation of safety reports (ICSRs – Individual Case Safety Reports)
- Perform basic literature searches for drug safety information
- Ensure compliance with regulatory guidelines (like ICH-GCP, FDA, EMA)
- Assist senior PV team in signal detection and safety review tasks
- Maintain documentation and audit-ready records
Pay: ₹15,000.00 - ₹27,000.00 per month
Benefits:
- Paid sick time
- Provident Fund
Work Location: In person
