Senior Clinical Research Associate

IQVIA UK

Manchester, United Kingdom
Site monitoring visits
Gcp and ich guidelines
Subject recruitment plan
Join IQVIA on our mission to accelerate innovation for a healthier world and strengthen our cFSP sponsor-dedicated team

Job Summary

  • Join IQVIA on our mission to accelerate innovation for a healthier world and strengthen our cFSP sponsor-dedicated team.
  • Perform site monitoring visits, administer protocol training, evaluate site practices, and manage study progress.
  • IQVIA is a 2026 "Glassdoor Best Place to Work in the UK" and recognized on the 2026 Fortune® World’s Most Admired Companies™ list.

Matching Summary

Join IQVIA on our mission to accelerate innovation for a healthier world and strengthen our cFSP sponsor-dedicated team.

Skills & Requirements

Must-have

  • Site monitoring visits
  • GCP and ICH guidelines
  • Subject recruitment plan
  • Protocol and study training
  • Quality and integrity evaluation
  • Trial Master File (TMF)

Nice-to-have

  • Innovative and curious mindset
  • Collaborative team environment
  • Agile career opportunities
  • Passion for work impact

Key Requirements

  • Experience of independent on-site monitoring
  • 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