Associate – Safety Data Management Specialist (Tamil Nadu)

Associate – Safety Data Management Specialist (Tamil Nadu)

08 Aug
|
Pfizer
|
Tamil Nadu

08 Aug

Pfizer

Tamil Nadu

Use Your Power for Purpose At Pfizer our Worldwide Medical and Safety colleagues are pivotal in bridging evidence-based medical decision support with stakeholders to enhance health and treatment outcomes Whether you are developing frameworks to ensure our evidence is scientifically robust offering unbiased and medically essential expertise or exploring ways to address data gaps our mission remains clear to empower healthcare decisions regarding the safe and appropriate use of medicines for patients Primary ResponsibilitiesCarry out case processing activities Review rank verify process and document case-related information event terms validity seriousness special scenarios timelines accuracy and consistency Process cases based on these assessments Review case criteria to determine appropriate workflow for case processing Assess cases to distinguish those with particular complexities and or specific issues and escalate appropriately Write and edit case narrative Determine and perform appropriate case follow-up including generation of follow-up requests Review processed cases to verify accuracy consistency and compliance with process requirements and review case data for special scenarios Liaise with key partners locally and other stakeholders regarding safety data collection and data reconciliation Develop and maintain expertise and knowledge for applicable corporate and global regulations for guidelines Standard Operating Procedures for data entry conventions and for search functions in the safety database Determine reportability of scheduled reports ensuring adherence to regulatory requirements Consistently apply regulatory requirements and Pfizer policies Participate as appropriate in local internal and external safety activities Here Is What You Need Minimum Requirements Education B Pharm M Pharm or Pharm D only Minimum experience 1 year Maximum 2 years Knowledge of ICSR processing Ability to work collaboratively in a team environment Bonus Points If You Have Preferred Requirements Hands on experience in ARGUS safety database Proficiency with processing source documents in XML format E2B R2 and R3 Good knowledge of medical terminology and global regulatory requirements for drug safety Work Location Assignment Hybrid Work Location Assignment Hybrid Pfizer is an equal chance employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates Medical

📌 Associate – Safety Data Management Specialist (Tamil Nadu)
🏢 Pfizer
📍 Tamil Nadu

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