Experienced Clinical Research Associate

IQVIA UK

Reading, United Kingdom
Independent on-site monitoring
Manage multiple clinical trial protocols
Knowledge of gcp and ich guidelines
Join IQVIA on our mission to accelerate innovation for a healthier world!

Job Summary

  • Join IQVIA on our mission to accelerate innovation for a healthier world!
  • You will perform site monitoring visits in accordance with regulatory requirements.
  • IQVIA is recognized as a top employer and values continuous learning.

Matching Summary

Join IQVIA on our mission to accelerate innovation for a healthier world!

Skills & Requirements

Must-have

  • independent on-site monitoring
  • manage multiple clinical trial protocols
  • knowledge of GCP and ICH guidelines

Nice-to-have

  • passion for innovation
  • collaborative team environment
  • commitment to growth

Key Requirements

  • life science degree or equivalent experience
  • flexibility to travel to sites

Work Rights

Not specified

Tailored Resume

Cover Letter