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✅ Pfizer Hiring Safety Data Management Associate – Apply Now (1–2 Yrs, Chennai)
📍 Location: Chennai (Hybrid)
🎓 Eligibility: B.Pharm, M.Pharm, Pharm.D
🧪 Experience: 1–2 Years (ICSR Processing)
💰 Salary: ₹6–8 LPA (Estimated)
📝 Job Type: Full-Time | Pharmacovigilance | Drug Safety
🔎 Verified: ✅ Verified Job via Medical Jobs India – hitechplus.in
🏢 About Pfizer
Pfizer is a globally renowned pharmaceutical company committed to breakthroughs that change patients' lives. With a strong focus on innovation and public health, Pfizer supports talent development and high-impact drug safety operations worldwide.
📄 Job Overview – Safety Data Management Associate
- Process adverse event cases, assess seriousness, and determine regulatory reportability.
- Write/edit case narratives and follow-up requests to ensure accurate data collection.
- Ensure adherence to ICSR processes including listedness, source validation, and ARGUS safety database usage.
- Collaborate with global safety teams for reconciliation and case review.
- Stay current with SOPs, E2B formats, GVP guidelines, and Pfizer standards.
✅ Eligibility & Skills
- Bachelor’s or Master’s degree in Pharmacy / Pharm.D
- 1–2 years’ experience in Pharmacovigilance (ICSR, ARGUS preferred)
- Familiarity with medical terminology, regulatory safety standards, XML formats
- Strong problem-solving, attention to detail, and communication skills
🎁 Why Join Pfizer
- 🌐 Work with global pharmacovigilance teams and cutting-edge safety systems
- 📈 Excellent opportunities for growth in drug safety and compliance
- 🏠 Hybrid work environment in Chennai
- 🤝 Inclusive culture and employee-first policies
📌 Note Before You Apply:
Highlight your experience in ICSR case processing, ARGUS, and XML/E2B standards in your resume for better shortlisting.
👇 Application Link Will Be Visible in 15 Seconds 👇
🟢 Verified Job via Medical Jobs India – hitechplus.in
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