Assoc Medical Safety Dir

IQVIA UK

Medical expertise
Pharmacovigilance
Adverse event review
Provide medical expertise on pharmacovigilance services to divisions as requested

Job Summary

  • Provide medical expertise on pharmacovigilance services to divisions as requested.
  • Perform medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs).
  • Ensure coverage for all medical safety deliverables within regulatory or contracted timelines.

Matching Summary

Provide medical expertise on pharmacovigilance services to divisions as requested.

Skills & Requirements

Must-have

  • medical expertise
  • pharmacovigilance
  • adverse event review
  • safety profile oversight
  • regulatory compliance

Nice-to-have

  • internal consulting
  • client meeting representation
  • industry development awareness

Key Requirements

  • Medical degree from accredited school
  • 3 years clinical practice experience
  • 2 years pharmaceutical industry experience
  • Knowledge of clinical trial regulations
  • Ability to establish and meet priorities

Work Rights

Not specified

Tailored Resume

Cover Letter