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), Positive 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
Perks:
Cell phone reimbursement
Paid sick time
Paid time off
Provident Fund
Work Location: In person
📌 Pharmacovigilance Associate Pune
🏢 Cliniweb Services
📍 Pune
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