Assoc Medical Safety Dir

IQVIA

Thane, India
Medical expertise on pharmacovigilance
Medical review of adverse events
Aggregate safety information 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 on pharmacovigilance
  • Medical review of adverse events
  • Aggregate safety information review
  • Coding review of medical data
  • Oversight of product safety profile
  • Client meeting representation

Nice-to-have

  • Internal consultant to case processing
  • Awareness of industry developments
  • Initiative and flexibility

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter