Pfizer — Safety Data Management Specialist

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Date: 15 hours ago
City: Makati City
Contract type: Full time
Job Description

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.

Tagged As

  • Clinical
  • Research
  • Biotech
  • Healthtech
  • Information Technology
  • Oncology
  • Big Data Analytics
  • AdTech
  • Digital Media
  • Software
  • Generative AI

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