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Associate Safety Data Management Specialist

Associate Safety Data Management Specialist

Pfizer

3 - 5 years

4 - 9 Lacs

chennai

Posted:3 days ago| Platform:

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Skills Required

analytical skills data management compliance coding xml clinical trials database pharmacovigilance drug safety

Work Mode

Work from Office

Job Type

Full Time

Job Description

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

Here Is What You Need (Minimum Requirements):

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.

Bonus Points If You Have (Preferred Requirements):

Course completion and/or certification in Pharmacovigilance or good knowledge of medical terminology and global regulatory requirements for drug safety.

Publications in peer reviewed journals.

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Pfizer

Pharmaceutical Manufacturing

New York New York

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Associate Safety Data Management Specialist