="text-align: center;">Pharm D Jobs at Pfizer | MPharma Candidates Apply Now for the Hybrid Position
Are you looking to advance your pharmaceutical career in drug safety? Pfizer is hiring an Associate – Safety Data Management Specialist in Chennai, where you will play a vital role in processing safety cases, ensuring regulatory compliance, and safeguarding patient well-being. This position offers an opportunity to work with global safety teams, develop expertise in safety databases, and contribute to high-quality pharmacovigilance operations.
About Pfizer
Pfizer is looking for an Associate – Safety Data Management Specialist to join its Worldwide Medical and Safety team in Chennai. In this role, you will be responsible for processing individual case safety reports (ICSRs), ensuring accuracy, regulatory compliance, and timely reporting. You will assess and document case-related information, manage follow-ups, and collaborate with global teams to support patient safety. This position offers the opportunity to work with advanced safety databases, apply your pharmaceutical expertise, and contribute directly to safeguarding patient health worldwide.
Job Details
- Job Post: Associate – Safety Data Management Specialist
- Job Requisition Id: 4939465
- Work Location: Hybrid – Chennai, India
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Requirements
- Education: B. Pharm, M. Pharm, or Pharm. D (mandatory).
- Experience: 1–2 years in end-to-end ICSR processing, including listedness assessment.
- Strong teamwork and collaboration skills.
Preferred Qualifications
- Experience with the ARGUS safety database.
- Proficiency with XML format processing (E2B R2 & R3).
- Knowledge of medical terminology and global regulatory requirements for drug safety.
About the Job
Pfizer is seeking a skilled Associate – Safety Data Management Specialist to join our Worldwide Medical and Safety team in Chennai. In this role, you will ensure the safe and appropriate use of medicines through accurate case processing, regulatory compliance, and collaboration with global teams.
Key Responsibilities:
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Process safety cases, review event terms, assess the seriousness of incidents, and document details with accuracy and consistency.
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Review case criteria, determine appropriate workflows, and escalate complex cases when necessary.
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Write and edit case narratives, perform follow-ups, and ensure compliance with regulatory requirements.
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Liaise with local and global partners to collect and reconcile safety data.
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Maintain expertise in corporate and global regulations, SOPs, and safety database processes.
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Determine the reportability of scheduled reports and ensure adherence to Pfizer policies.
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Participate in internal and external safety activities as appropriate.
- Pfizer is an equal opportunity employer, committed to diversity, equity, and inclusion in all our workplaces.
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