Experienced Clinical Research Associate

IQVIA Inc

United Kingdom
Independent on-site monitoring experience
Good clinical practice (gcp) knowledge
Ich guidelines expertise
The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with GCP and ICH guidelines

Job Summary

  • The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with GCP and ICH guidelines.
  • Candidates will work with sites to adapt, drive, and track subject recruitment plans to enhance predictability and manage ongoing project expectations.
  • IQVIA is recognized as a #1 company in its category on the Fortune World's Most Admired Companies list for the fifth consecutive year.

Matching Summary

The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with GCP and ICH guidelines.

Skills & Requirements

Must-have

  • Independent on-site monitoring experience
  • Good Clinical Practice (GCP) knowledge
  • ICH guidelines expertise
  • Multiple clinical trial protocol management
  • Site recruitment plan tracking

Nice-to-have

  • Agile career opportunities
  • Collaborative team environment
  • Innovative problem solving
  • Commitment to continuous learning

Key Requirements

  • Life science degree or equivalent industry experience
  • Flexibility to travel to sites
  • UK work authorization required (no visa sponsorship)

Work Rights

Must have UK work authorization

Tailored Resume

Cover Letter