Pfizer is the world's premier biopharmaceutical company taking new approaches to better health. We discover, develop, manufacture and deliver quality, safe and effective prescription medicines to treat and help prevent disease for both people and animals. We also partner with healthcare providers, governments and local communities around the world to expand access to our medicines and to provide better quality health care and health system support.
Post : Associate Safety Data Management Specialist
Job Description
In this pharmacovigilance role, you will carry out processing activities of Individual Case Safety Reports (both clinical trials and post-marketing sources) in the ARGUS Safety database.
Processing activities include assessing case validity, undertaking duplicate checks, creating cases in the database, prioritizing cases as per company guidance, updating cases with information provided in XML source documents, identifying adverse events, confirming their seriousness, coding products, undertaking causality and listedness assessments, drafting narratives, determining appropriate case follow-up, reviewing processed cases to verify technical judgment, accuracy, and compliance with company requirements, etc.
Candidate Profile
Education = B. Pharm, M. Pharm, or Pharm. D only.
Experience = FRESHERS ONLY!
Keen attention to detail.
Solid analytical skills.
Good written and oral communication skills.
Collaborative skills.
Continuous Learning.
Additional Information
Experience : FRESHERS ONLY
Qualification : B.Pharm, M.Pharm, or Pharm.D
Location : Chennai
Job ID : 4943867
Industry Type : Pharma/ Healthcare/ Clinical research
End Date : 30th October 2025
Data Management Specialist Apply Online
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