Experienced CRA – Clinical Research Associate ()


  • You are responsible for the management and monitoring of different phases, especially phase IV trials.
  • You act as the main line of communication between the sponsor and the investigator
  • You ensure delivery of high quality, clean CRFs by adherence to Good Clinical Practices and ensuring investigator compliance with protocol and study procedures
  • You ensure adequacy of clinical research staff/facilities in accordance with defined general (GCP/ Sops) and protocol-specific requirements
  • You ensure timely submission, initiation, monitoring and close-out
  • You ensures investigator completion and compilation of all necessary pre-trial documentation from the investigator site (e.g. signed protocol, Cvs, patient information and consent forms, ethics committee approval documents etc.)
  • You may Negotiate investigator grants within a protocol specific budget suggested by Clinical Operation Management
  • You perform and coordinate trial specific training for investigational site staff
  • Scientific Degree or experience in the conduct of clinical trials
  • A good knowledge of English, Dutch and French is an absolute requirement
  • Experience in a similar position is an absolute requirement
  • Experience with Microsoft based applications and general knowledge of PC functions
  • Able to take initiative and work independently
  • Team player
    • A contract of indefinite duration
    • The opportunity to develop your competences and grow your career within a dynamic and challenging leading company
    • You will receive an attractive salary with other advantages as e.g. group insurance, hospitalization insurance, meal vouchers, Company Car, …
    • You will have the ability to work partially home based



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