Primary Responsibilities  

Carry 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.End to End ICSR processing, including listedness assessment.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

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

Medical

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