Empower healthcare decisions by ensuring the safe and appropriate use of medicines for patients. Review and complete reports of adverse drug experiences to determine the safety profile of Pfizer’s products and meet regulatory requirements.
Requirements
Review, preparation, and completion of reports of adverse drug experiences
Identify and select routine cases for processing
Assess cases to distinguish those with particular complexities and/or specific issues
Review, rank, verify, process and document case information
Generate reports, ensuring adherence to regulatory compliance timelines
Determine appropriate case follow-up, requesting follow-up letters when appropriate
Liaise with key partners regarding safety data collection and data reconciliation
Develop and maintain expertise and knowledge of all products within the Pfizer portfolio
Consistently apply regulatory requirements and Pfizer policies
Benefits
Hybrid work location assignment
Opportunity to develop expertise and knowledge of all products within the Pfizer portfolio
Consistent application of regulatory requirements and Pfizer policies
