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Pfizer, a global leader in pharmaceuticals, is inviting applications for the position of Associate – Safety Data Management Specialist in Chennai, India. This role is ideal for B.Pharm, M.Pharm, or Pharm.D graduates passionate about pharmacovigilance and drug safety data management.
If you have experience in ICSR case processing, a strong grasp of global safety regulations, and want to contribute to patient safety, this position offers the perfect career advancement.
💼 Job Responsibilities
As a Safety Data Management Specialist at Pfizer, you will:
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- Perform case processing and documentation of safety data.
- Review, rank, verify, and process case-related information for accuracy and compliance.
- Assess validity, seriousness, and timelines of cases.
- Draft and edit case narratives and follow up on incomplete information.
- Collaborate with global safety teams and key partners for data reconciliation.
- Maintain up-to-date knowledge of ICSR guidelines, SOPs, and regulatory standards.
- Ensure compliance with Pfizer policies and global pharmacovigilance regulations.
- Participate in local and international safety review meetings as needed.
🎓 Required Qualifications
- Education: B.Pharm, M.Pharm, or Pharm.D (mandatory).
- Experience: 1–2 years in pharmacovigilance or drug safety.
- Skills:
- Solid understanding of ICSR processing.
- Strong analytical and documentation skills.
- Ability to work collaboratively in a team environment.
🌟 Preferred Qualifications
- Hands-on experience in ARGUS Safety Database.
- Familiarity with E2B (R2/R3) XML source document processing.
- Proficiency in medical terminology and regulatory compliance standards.
🏢 Job Location & Type
- Location: Chennai, India
- Work Type: Full-time (Hybrid work model)
- Organization: Pfizer
💰 Salary Range
Competitive — ₹4,00,000 to ₹6,50,000 per annum, depending on experience and qualifications.
✉️ How to Apply
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