Cra2 - Multi-sponsor Department

IQVIA UK

Independent on-site monitoring experience
Knowledge of good clinical practice guidelines
Experience managing multiple clinical trial protocols
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 and track subject recruitment plans while ensuring the integrity of study practices.
  • IQVIA offers a career with greater purpose where employees can make an impact and never stop learning.

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
  • Knowledge of Good Clinical Practice guidelines
  • Experience managing multiple clinical trial protocols

Nice-to-have

  • Flexibility to travel to sites
  • Strong communication skills with sites
  • Ability to drive subject recruitment plans

Key Requirements

  • Life science degree or equivalent industry experience
  • Experience of independent on-site monitoring
  • UK work authorization required (no visa sponsorship)

Work Rights

Must have UK work authorization

Tailored Resume

Cover Letter