Pharmacovigilance Analyst

1 month ago

Pune, Maharashtra, India EVERSANA Full time
Job Description

This role requires in-depth knowledge of the scientific basis for therapies and drug-induced diseases, as well as familiarity with product portfolios and safety profiles across therapeutic areas.

  • Perform medical review of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs)
  • Compose, edit, and medically review Analyses of Similar Events (AOSE) for expedited cases as appropriate based on regulatory requirements
  • Serve as an internal consultant to pharmacovigilance case processing teams on projects being supported

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