Pfizer — Safety Data Management Specialist

Pfizer — Safety Data Management Specialist

Location: Makati City, Metro Manila (Hybrid)

Level: Junior

Industry: Pharma, HealthTech, AI, Machine Learning, Biotech

Role Overview

Monitor adverse drug and device reports, support clinical trial and post-marketing safety activities, and ensure compliance with regulatory requirements. Help maintain Pfizer’s safety surveillance program by reviewing and processing safety data.

Key Responsibilities

• Process and review adverse event cases for validity, seriousness, and accuracy.
• Write/edit case narratives and perform follow-ups as needed.
• Determine appropriate workflows and escalate complex cases.
• Collaborate with internal teams and external partners on safety data collection and reconciliation.
• Maintain knowledge of regulatory requirements, SOPs, and data entry conventions.
• Determine reportability and ensure compliance with safety reporting regulations.
• Support safety-related activities both locally and globally.

Qualifications & Skills

• Bachelor’s degree in Health or Life Sciences.
• 1+ year preferred experience in pharmacovigilance or data management.
• Medical writing skills are a plus.
• Familiarity with relational databases and computer literacy required.
• Ability to solve routine problems with supervision and work effectively in a matrix environment.
• Fluent in English, both spoken and written.

Work Environment

• On-premise role with no relocation support.
• Pfizer is an equal opportunity employer.