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  • Location:

    Vilvoorde, Belgium

  • Contact:

    Nele Daems

  • Job type:


  • Contact phone:

    015 858038

  • Industry:


  • Contact email:

For one of our clients we are looking for an experienced CRA.  You will have the ability to work directly for the sponsor, one of the top 10 pharmaceutical companies in Belgium.  Together with the client, Oxford will guide & support you intensively the first months by means of coaching on the job.

Job Description

Perform all required activities to ensure appropriate monitoring of investigator sites and trial execution. Primary person responsible for management of assigned sites, including acting as central point of communication between client and Investigator sites.


  • Perform monitoring visits according to monitoring plan (including trial initiation, training and closeout activities)
  • Participate in site nomination process, perform evaluation of site capability and make recommendation for inclusion in clinical trial
  • Point of contact for sites and facilitator of communication between sites and key line functions
  • Ensure preparation, collection and distribution of trial master file documents and maintenance of investigator site file
  • Timely write-up of study monitoring visit reports
  • Set up and ensure maintenance of investigator site file
  • Manage site vaccine supply and sample management during course of study
  • Ensure site performance in line with milestones and KPI’s (i.e. start-up, recruitment, closeout, etc.)
  • Support investigator in implementing appropriate contingency plans as needed


  • A first experience as CRA
  • Master degree in science related field
  • Knowledge of Office
  • Strong verbal communications skills
  • Good cooperative and collaborative skills
  • Dutch/English/French knowledge