Independent Drug Monitoring Manager - Sponsor Dedicated

IQVIA

6 years clinical trial operations experience
Unblinded drug management expertise
Ich-gcp and regulatory compliance knowledge
This home-based role provides global coordination for unblinded drug management and the Independent Drug Monitoring process within the EMEA region

Job Summary

  • This home-based role provides global coordination for unblinded drug management and the Independent Drug Monitoring process within the EMEA region.
  • The candidate must ensure inspection readiness by strictly adhering to SOPs, GCP codes, and local regulations from study start-up through close-out.
  • Key responsibilities include leading study teams, managing IDMs, resolving critical pharmacy issues, and maintaining unblinded data integrity.

Matching Summary

This home-based role provides global coordination for unblinded drug management and the Independent Drug Monitoring process within the EMEA region.

Skills & Requirements

Must-have

  • 6 years clinical trial operations experience
  • Unblinded drug management expertise
  • ICH-GCP and regulatory compliance knowledge
  • Global scope or global mindset
  • Project management skills
  • IDM team leadership and coordination

Nice-to-have

  • Monitoring experience preferred
  • International environment work history
  • Database lock and interim analysis support
  • Training and coaching capabilities
  • Strong analytical and decision-making skills

Key Requirements

  • Bachelor's degree in scientific or business discipline
  • 6 years relevant experience in pharmaceutical industry or CRO
  • Proficiency in English and local country language
  • Willingness to travel locally/domestically
  • Not eligible for UK visa sponsorship

Work Rights

Not specified

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