Safety Data Management Specialist

Position Purpose

Review, preparation, and completion of reports of adverse drug experiences, to determine the safety profile of Pfizer’s products and to meet regulatory requirements. Determination of local submission of individual and, where appropriate, aggregate safety reports.

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 assessments and determine appropriate workflow.
• Assess cases to distinguish those with particular complexities and/or specific issues and escalated 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 requirement...