Senior Pharmacovigilance Associate

ICON Clinical Research, LP

Manila, Philippines
Hybrid
Medical review of adverse event reports
Icsr medical reviews
Safety database experience
As a Senior Pharmacovigilance Associate at ICON, you will play a pivotal role in overseeing the medical aspects of pharmacovigilance activities, ensuring the safety of investigational drugs and contributing to the advancement of innovative treatments and therapies

Job Summary

  • As a Senior Pharmacovigilance Associate at ICON, you will play a pivotal role in overseeing the medical aspects of pharmacovigilance activities, ensuring the safety of investigational drugs and contributing to the advancement of innovative treatments and therapies.
  • This role is responsible for conducting comprehensive medical review of Individual Case Safety Reports (ICSRs), ensuring the accuracy, integrity, and compliance of global regulatory reports, and for collaborating cross functionally and providing technical leadership within Case Management and across Global Patient Safety (GPS).
  • In addition to your competitive salary, ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities for you and your family.

Matching Summary

As a Senior Pharmacovigilance Associate at ICON, you will play a pivotal role in overseeing the medical aspects of pharmacovigilance activities, ensuring the safety of investigational drugs and contributing to the advancement of innovative treatments and therapies.

Skills & Requirements

Must-have

  • Medical review of adverse event reports
  • ICSR medical reviews
  • Safety database experience
  • Fluent in English

Nice-to-have

  • Cross-functional collaboration
  • Technical leadership
  • Risk management strategies
  • Fast-paced matrixed environment

Key Requirements

  • BS degree in health-related or scientific field
  • 3-5 years clinical experience
  • 2-5 years pharmaceutical experience
  • At least 2 years clinical development experience
  • Safety case processing experience required
  • Exposure to safety database (ARGUS preferred)
  • Strong clinical/diagnostic skills
  • Excellent interpersonal, organizational and negotiation skills
  • Ability to work on multiple projects
  • Ability to prioritize tasks and shift priorities rapidly
  • Ability to influence others

Work Rights

Not specified

Tailored Resume

Cover Letter