Experienced Clinical Research Associate - Ireland

IQVIA Inc

Republic of Ireland
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 while ensuring data integrity.

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 and initiation visits
  • Subject recruitment plan management

Nice-to-have

  • Life science degree education
  • Experience with diverse investigative sites
  • Flexibility to travel to sites
  • Strong communication skills
  • Data query resolution experience

Key Requirements

  • Minimum 18 months of independent on-site monitoring
  • Successfully managed multiple clinical trial protocols
  • In-depth knowledge of Good Clinical Practice (GCP)
  • In-depth knowledge of International Conference on Harmonization (ICH) guidelines
  • Life science degree or equivalent industry experience
  • Not eligible for UK visa sponsorship

Work Rights

Must be eligible to work in Ireland; not eligible for UK visa sponsorship

Tailored Resume

Cover Letter