Clinical Research Associate (CRA)

Scope of the Job

The CRA is responsible for “on-site” quality control of clinical trials to ensure that a clinical trial is conducted, recorded and reported in accordance with the protocol, the principles of Good Clinical Practice (GCP) and the applicable regulatory requirements.

Main responsibilities / Major Activities

  • Perform on-site monitoring visits according to the monitoring plan and following the EORTC Standard Operating procedures (SOPs) and ICH-GCP guidelines
  • Ensure and control sites’ compliance with study protocol and regulatory obligations
  • Address issues in a manner that is beneficial for the site and the EORTC team
  • Report the findings of the “on-site” monitoring visits according to EORTC Standards
  • Follow the sites’ findings until resolution, with the support of the EORTC study team and Quality Assurance and Control unit
  • Perform site staff training whenever needed during the study conduct
  • Ensure close collaboration between all actors of clinical trial research, as a privilege link between investigational sites and the EORTC study team


  • University degree or equivalent in Health Sciences
  • Practical knowledge of the conduct of clinical trials
  • Prior experience of at least 2 years as CRA
  • Prior experience in Oncology
  • Ability to travel 40% of working time across European countries


  • Languages: English (written & spoken) is mandatory, and Dutch. Any other EU language is an asset (French, German, Italian, Spanish).
  • Excellent organization
  • Good communication skills
  • Proactive, dynamic
  • Independent and team-player
  • Flexible attitude with respect to work assignments and new learning

Application form

*Compulsary fields
Application should be sent in English

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