Collect, review, and process adverse event reports from healthcare professionals, patients, and clinical studies.
Enter and maintain accurate case data in safety databases.
Perform case assessment and narrative writing under supervision.
Assist in the preparation of Individual Case Safety Reports (ICSRs) and follow-up activities.
Support signal detection and risk assessment processes.
Ensure compliance with global pharmacovigilance regulations and company SOPs.
Coordinate with cross-functional teams such as regulatory affairs, medical affairs, and clinical research.
Participate in audits and inspections as needed.
Job Types: Full-time, Permanent, Fresher
Pay: ?261,554.81 - ?581,394.30 per year
Benefits:
Health insurance
Paid sick time
Paid time off
Provident Fund
Work Location: In person
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