
Pfizer — Safety Data Management Specialist
3 days ago
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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