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Clinical Research Associate (Belgium)

  • A hirdetés 1204 napja lejárt

Fixed term contract for 2 years.

For our partner located in Belgium, we are looking for a Clinical Research Associate, who will be 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

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


  • University degree in Health Sciences, or equivalent areas
  • Practical knowledge of the conduct of clinical trials
  • Prior experience of at least 1 year in Clinical Research (monitor, data manager, or research nurse)
  • Experience in Oncology is an advantage
  • Languages:
    English: excellent level is required (written & spoken)
    German: good level is required (written & spoken)
  • Excellent organization and communication skills
  • Proactive, dynamic
  • Flexible attitude with respect to work assignments and new learning
  • Ability to travel an average of 40% within European countries
  • Available immediately
If you are interested, please send your CV and cover letter to Ines Pereira to the following e-mail address: E-mail cím megjelenítése.

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