Clinical Research Associate

IQVIA UK

United Kingdom
Oncology studies monitoring
Site monitoring visits
Gcp and ich guidelines knowledge
The Clinical Research Associate will support Oncology studies and cover sites across the UK

Job Summary

  • The Clinical Research Associate will support Oncology studies and cover sites across the UK.
  • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
  • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution.

Matching Summary

The Clinical Research Associate will support Oncology studies and cover sites across the UK.

Skills & Requirements

Must-have

  • Oncology studies monitoring
  • Site monitoring visits
  • GCP and ICH guidelines knowledge
  • Subject recruitment plan tracking
  • Protocol and study training administration

Nice-to-have

  • Collaborate with study team members
  • Enhance predictability of recruitment
  • Forge a career with greater purpose

Key Requirements

  • Experience of independent on-site monitoring
  • Life science degree educated or equivalent
  • Flexibility to travel to sites

Work Rights

Not specified

Tailored Resume

Cover Letter