Senior Clinical Research Associate, Oncology

IQVIA UK

Manchester, United Kingdom
Independent on-site monitoring
Knowledge of gcp and ich guidelines
Experience managing clinical trial protocols
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 workplace in the UK.

Matching Summary

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

Skills & Requirements

Must-have

  • Independent on-site monitoring
  • Knowledge of GCP and ICH guidelines
  • Experience managing clinical trial protocols

Nice-to-have

  • Flexibility to travel
  • Strong communication skills
  • Team collaboration

Key Requirements

  • Life science degree or equivalent experience
  • Experience with subject recruitment plans
  • Ability to track regulatory submissions

Work Rights

Not specified

Tailored Resume

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