- Review and process Individual Case Safety Reports (ICSRs).
- Collect, document, and evaluate adverse event information from various sources.
- Perform data entry into pharmacovigilance safety databases.
- Ensure accuracy, completeness, and quality of case processing.
- Conduct medical literature screening for safety-related information.
- Follow Standard Operating Procedures (SOPs), Good Pharmacovigilance Practices (GVP), and regulatory guidelines.
- Support case follow-up activities to obtain complete safety information.
- Assist in preparing periodic safety reports and other regulatory documentation.
- Maintain confidentiality and data integrity throughout all activities.
- Collaborate with internal teams to ensure timely case submission.
Pay: ₹18,000.33 - ₹30,000.79 per month
Benefits:
- Cell phone reimbursement
- Paid sick time
- Paid time off
- Provident Fund
Work Location: In person
