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Pfizer Hiring Safety Data Management Specialist
Pfizer
Chennai
0–2 Years
Pharmacovigilance
ICSR
🏢 About Pfizer
Pfizer is a global biopharmaceutical leader focused on breakthrough therapies in vaccines, oncology, rare diseases, and internal medicine. The company promotes innovation, diversity, and strong career growth in healthcare and drug safety.
📌 Job Overview
- Role: Associate – Safety Data Management Specialist
- Location: Chennai (Hybrid)
- Experience: 0–2 Years
- Job ID: 4953942 / 4953995
- Department: Pharmacovigilance
🎯 Key Responsibilities
- Process Individual Case Safety Reports (ICSR)
- Assess case validity, seriousness & reportability
- Write and review case narratives
- Perform follow-ups and query generation
- Ensure data consistency and compliance
- Collaborate with global PV teams
- Support audits and inspections
🎓 Eligibility & Skills
- B.Pharm / M.Pharm / Pharm.D
- 0–2 years PV experience
- Knowledge of ICSR processing
- ARGUS database (preferred)
- E2B R2/R3 knowledge
- Medical terminology understanding
- Strong analytical & communication skills
⭐ Salary & Benefits
- Competitive salary (Pfizer standard)
- Hybrid work model
- Global pharmacovigilance exposure
- Career growth & learning programs
- Health insurance & employee benefits
🎯 Interview Preparation Tips
Must Prepare Topics:
- ICSR lifecycle (intake → processing → submission)
- Serious vs Non-serious cases
- MedDRA coding basics
- Listedness & expectedness
- E2B XML concepts
- ARGUS workflow basics
Helpful Resources:
📌 Note Before You Apply:
Ensure you have basic knowledge of pharmacovigilance and ICSR processing before applying.
Ensure you have basic knowledge of pharmacovigilance and ICSR processing before applying.
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