Associate Medical Safety Director

IQVIA

Bangalore, India
Medical expertise in safety data evaluation
Pharmacovigilance process
Aggregate safety reports
Provide medical expertise in the evaluation of safety data as part of the overall pharmacovigilance process

Job Summary

  • Provide medical expertise in the evaluation of safety data as part of the overall pharmacovigilance process.
  • Perform medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs).
  • Provide aggregate reviews of safety information to maintain oversight of a product’s safety profile.

Matching Summary

Provide medical expertise in the evaluation of safety data as part of the overall pharmacovigilance process.

Skills & Requirements

Must-have

  • Medical expertise in safety data evaluation
  • Pharmacovigilance process
  • Aggregate safety reports
  • Surveillance activities for products
  • Medical review of AEs and ADRs
  • Therapeutic area guidance

Nice-to-have

  • Internal consultant to pharmacovigilance teams
  • Lead and participate in training
  • Awareness of medical safety-regulatory developments
  • Signal detection efforts

Key Requirements

  • Medical degree from accredited medical school
  • 3 years clinical medicine experience
  • 2 years pharma experience
  • Valid medical license

Work Rights

Not specified

Tailored Resume

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