Experienced Clinical Research Associate

IQVIA

Reading, United Kingdom
Perform site monitoring visits
Manage clinical trial protocols
Adherence to 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!
  • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements.
  • IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

Matching Summary

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

Skills & Requirements

Must-have

  • Perform site monitoring visits
  • Manage clinical trial protocols
  • Adherence to GCP and ICH guidelines
  • Track subject recruitment plan
  • Evaluate site quality and integrity

Nice-to-have

  • Innovative and curious mindset
  • Collaborate and liaise with study team
  • Agile career opportunities

Key Requirements

  • Experience of independent on-site monitoring
  • Managed multiple clinical trial protocols
  • In depth knowledge of GCP and ICH
  • Life science degree or equivalent experience
  • Flexibility to travel to sites

Work Rights

Not specified

Tailored Resume

Cover Letter