Pfizer Hiring for Pharmacovigilance Job | Pharma Freshers Job |Associate Safety Data Management Specialist Role
Looking for a Pharma Job in Chennai with a global leader? This Pharma Freshers Job opportunity at Pfizer is perfect for candidates interested in pharmacovigilance and drug safety. Pfizer is hiring an Associate Safety Data Management Specialist to support safety data processing and regulatory compliance, offering excellent career growth in clinical safety and data management.
- Job Title: Associate Safety Data Management Specialist
- Location: India – Chennai
- Job Requisition ID:4953942
About the Company
Pfizer is one of the world’s leading biopharmaceutical companies focused on advancing health through innovative medicines and vaccines. Its Worldwide Medical and Safety teams play a crucial role in ensuring safe and effective use of medicines through evidence-based decision-making.
Key Responsibilities
- Monitor the company’s drug, biologics, and medical devices surveillance program.
- Intake, evaluate, and process adverse reports for both clinical trials and post-marketing activities.
- Make decisions within limited options to resolve problems, under the supervisor’s direction.
- Work in a structured environment, following established procedures.
- Ensure work is regularly reviewed for technical judgment, completeness, and accuracy.
- Provide expertise on regulatory requirements and corporate policies for regulatory submissions to project teams.
- Support the Worldwide Strategy and Regulatory teams by analyzing post-marketing safety data, reviewing medical literature, and related activities.
- Determine the appropriate workflow for case processing by reviewing case criteria.
- Carry out processing activities of Individual Case Safety Reports (ICSRs) in the ARGUS Safety database.
- Perform case validity assessment, duplicate checks, case creation, prioritization, and data updates.
- Identify adverse events, confirm seriousness, code products, and perform causality and listedness assessments.
- Draft narratives, determine follow-ups, and review processed cases for compliance and accuracy.
Qualification
- Education: B. Pharm, M. Pharm, or Pharm. D only.
- Experience: 0 to 2 years ONLY, please!
- Keen attention to detail.
- Solid analytical skills.
- Good written and oral communication skills.
- Collaborative skills.
- Continuous Learning.
Preferred Requirements
- Certification in Pharmacovigilance or knowledge of medical terminology and global drug safety regulations.
- Publications in peer-reviewed journals.
- Experience using AI tools such as ChatGPT or Microsoft Copilot.
- Understanding of responsible AI practices, including ethical use and risk management.
