Senior Clinical Research Associate

IQVIA

Manchester, United Kingdom
On-site monitoring experience
Gcp and ich guidelines
Site monitoring visits
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 2026 "Glassdoor Best Place to Work in the UK".

Matching Summary

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

Skills & Requirements

Must-have

  • On-site monitoring experience
  • GCP and ICH guidelines
  • Site monitoring visits
  • Protocol and study training
  • Subject recruitment plan

Nice-to-have

  • Innovative and curious mindset
  • Collaborative working style
  • Agile career opportunities
  • Passion for patient impact

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter