Cra2 - Multi-sponsor Department

IQVIA UK

United Kingdom
**
Perform site monitoring visits
Manage clinical trial protocols
Adhere to gcp and ich guidelines
** IQVIA UK is seeking both junior and experienced Clinical Research Associates (CRAs) for their growing multi-sponsor Site Management team. The position involves site monitoring, regulatory compliance, and collaboration with study teams to ensure successful clinical trials. **

Job Summary

  • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
  • 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.
  • Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.

Matching Summary

Match Score: 75

** IQVIA UK is seeking both junior and experienced Clinical Research Associates (CRAs) for their growing multi-sponsor Site Management team. The position involves site monitoring, regulatory compliance, and collaboration with study teams to ensure successful clinical trials. **

Skills & Requirements

Must-have

  • Perform site monitoring visits
  • Manage clinical trial protocols
  • Adhere to GCP and ICH guidelines
  • Track study progress and documentation
  • Collaborate with study team members

Nice-to-have

  • Forge a career with greater purpose
  • Make an impact and never stop learning

Key Requirements

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

Work Rights

Not specified

Tailored Resume

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