Perform case intake of Individual Case Safety Reports (ICSRs) from various sources (patients, healthcare professionals, literature, etc.).
Enter and update safety data accurately in pharmacovigilance databases.
Conduct initial assessment and triage of reported adverse events.
Assist in coding medical terms using MedDRA.
Ensure timely and compliant reporting of safety cases to regulatory authorities.
Support preparation of safety narratives and case summaries under supervision.
Review source documents for accuracy and completeness.
Assist with signal detection and ongoing safety monitoring activities.
Follow SOPs, GVP guidelines, and global regulatory requirements.
Collaborate with cross-functional teams (clinical, regulatory, quality) as needed.
Job Types: Full-time, Permanent, Fresher
Pay: ?304,180.41 - ?657,797.04 per year
Benefits:
Cell phone reimbursement
Food provided
Health insurance
Paid sick time
Provident Fund
Work from home
Work Location: In person
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