Senior Clinical Research Associate

IQVIA

UK
18 months independent on-site monitoring experience
Good clinical practice gcp knowledge
Ich guidelines expertise
IQVIA is recognized as #1 in its category on the 2026 Fortune World's Most Admired Companies list for the fifth consecutive year

Job Summary

  • IQVIA is recognized as #1 in its category on the 2026 Fortune World's Most Admired Companies list for the fifth consecutive year.
  • 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 project performance.

Matching Summary

IQVIA is recognized as #1 in its category on the 2026 Fortune World's Most Admired Companies list for the fifth consecutive year.

Skills & Requirements

Must-have

  • 18 months independent on-site monitoring experience
  • Good Clinical Practice GCP knowledge
  • ICH guidelines expertise
  • Site selection initiation and close-out visits
  • Subject recruitment plan management

Nice-to-have

  • Life science degree education
  • Flexible to travel to sites
  • Collaborative study team support
  • Cutting edge medicines development exposure

Key Requirements

  • Minimum 18 months independent on-site monitoring
  • Successfully managed multiple clinical trial protocols
  • In-depth knowledge of GCP and ICH guidelines
  • Life science degree or equivalent industry experience
  • Not eligible for UK visa sponsorship

Work Rights

Must have UK work authorization

Tailored Resume

Cover Letter