Cta 2

IQVIA UK

Netherlands
Maintain clinical documents and systems
Prepare and file clinical documentation
Track clinical data flow
Perform daily administrative activities in conjunction with Clinical Research Associates and Regulatory and Start-Up teams to ensure a complete and accurate Trial Master File delivery

Job Summary

  • Perform daily administrative activities in conjunction with Clinical Research Associates and Regulatory and Start-Up teams to ensure a complete and accurate Trial Master File delivery.
  • Assist CRAs and RSU with accurately updating and maintaining clinical documents and systems that track site compliance and performance within project timelines.
  • Coordinate the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.

Matching Summary

Perform daily administrative activities in conjunction with Clinical Research Associates and Regulatory and Start-Up teams to ensure a complete and accurate Trial Master File delivery.

Skills & Requirements

Must-have

  • Maintain clinical documents and systems
  • Prepare and file clinical documentation
  • Track clinical data flow
  • Central contact for clinical team

Nice-to-have

  • Assist with site visits
  • Collaborate with clinical team

Key Requirements

  • Bachelor's Diploma or equivalent
  • 3-4 years administrative support experience
  • Excellent command of Dutch and English languages
  • Working knowledge of Microsoft Office Suite
  • Basic knowledge of GCP and ICH guidelines

Work Rights

Must be based in the Netherlands

Tailored Resume

Cover Letter