Are you a B.Pharm, M.Pharm, or Pharm.D graduate eager to begin your career in pharmacovigilance? Here’s your chance to join one of the world’s most trusted pharmaceutical companies — Pfizer. This entry-level pharmacovigilance job in Chennai offers hands-on exposure to drug safety data management using the ARGUS Safety database, providing a solid foundation for your journey in clinical safety.
About the Role
As an Associate Safety Data Management Specialist, you will handle and process Individual Case Safety Reports (ICSRs) from both clinical trials and post-marketing sources. This role focuses on ensuring compliance, accuracy, and scientific precision in drug safety reporting.
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Key Responsibilities
- Process and assess case validity in the ARGUS Safety Database.
- Conduct duplicate checks and case creation for ICSR submissions.
- Identify adverse events and assess their seriousness and causality.
- Perform medical coding for drugs and events using global standards.
- Draft detailed narratives and follow-up reports.
- Ensure accuracy, completeness, and adherence to Pfizer’s safety protocols.
- Review processed cases to maintain technical and regulatory compliance.
Qualifications & Requirements
Minimum Requirements
- Education: B.Pharm, M.Pharm, or Pharm.D.
- Freshers only (no prior experience required).
- Excellent analytical, communication, and collaboration skills.
- Strong attention to detail and ability to learn continuously.
Preferred Skills
- Certification in Pharmacovigilance or Drug Safety.
- Knowledge of medical terminology and global PV regulations.
- Publications or academic experience in clinical or pharmaceutical sciences.
Why Join Pfizer?
- Work with a global leader in healthcare innovation.
- Gain real-time experience with the ARGUS Safety Database.
- Hybrid work model for better work-life balance.
- Excellent platform for career growth in pharmacovigilance.
- Inclusive workplace that values diversity and collaboration.
Work Location
📍 Location: Chennai, India
🏠 Work Mode: Hybrid
How to Apply
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