Associate Medical Safety Director

IQVIA UK

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

Job Summary

  • Provide medical expertise in the evaluation of safety data from a variety of sources 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 from a variety of sources as part of the overall pharmacovigilance process.

Skills & Requirements

Must-have

  • Medical safety data evaluation
  • Pharmacovigilance process
  • Aggregate safety reports
  • Protocol and CRF review
  • Signal detection efforts

Nice-to-have

  • Senior technical leader
  • Matrix management activities
  • Client meeting representation
  • Medical escalation support

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter