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Pharmacovigilance Specialist (Taguig) | Hybrid

TaguigHybridFull-time

AI Summary

Pharmacovigilance Specialist processes safety cases, including book-in, data entry, narrative writing, medical/product coding, quality checks, and case routing/closure in a hybrid role based in Taguig.

About this role

Work Setup: Willing to work full onsite during training and hybrid (3x onsite per week) upon production in Taguig

Start Date: Nov 3, 2026

Requirements:

  • Pharmacy Graduates required with or without active license
  • Nursing Graduates will be considered
  • 1 to 2 years of safety case processing experience in Pharmacovigilance Safety databases like Veeva Safety Database, Argus.
  • Good communication skills
  • Willing to work full onsite during training and hybrid (3x onsite per week) upon production in Taguig

Key Responsibilities:

  • Case Processing: Perform book-in, data entry, and narrative writing.
  • Coding: Handle medical and product coding.
  • Quality Control: Conduct quality checks using online tools.
  • Workflow Management: Manage case routing, closure, and USPI labeling.

Skills

ArgusCase ClosureCase ProcessingCase RoutingMedical CodingNarrative WritingProduct CodingQuality ControlUSPI LabelingVeeva Safety Database

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