Covance

  • (Senior) Clinical Research Associate, Brussels

    Job Location(s) BE-Brussels
    Job Number
    2018-18036
    Job Category
    Clinical Research Associate
    Position Type
    Full-Time
  • Job Overview

    We are currently looking for a talented Clinical Research Associates to join Covance in Belgium! This is a Sponsor dedicated position which will give you the opportunity to work with and for one of the most innovative pharmaceutical company in the industry. 

     

    You will be part of a great and dynamic team, with the possibility to devote all your professional skills and knowledge into monitoring investigational sites as we organize our work environment and responsibilities with high standards.

     

    Location: Brussels / Home-Based possible with presence required in client offices on a regular basis

     

    This is time to join our EMEA FSPx Team! 

    Education / Qualifications

    • University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology)
    • In lieu of the above requirement, candidates with three (3) or more years of relevant clinical research experience in pharmaceutical or CRO industries may be considered
    • Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements
    • Thorough knowledge of monitoring procedures
    • Basic understanding of the clinical trial process

    Experience

      • Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines
      • Have a full understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
      • Good planning, organization and problem solving abilities
      • Ability to work with minimal supervision
      • Good communication and interpersonal skills
      • Good analytical and negotiation skills
      • Computer competency
      • Fluent in local office language and in English, both written and verbal
      • Works efficiently and effectively in a matrix environment
      •  Minimum of two (2) years of clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits)

    Apply now and join us! 

     

    Key words:

     

    Clinical Research, CRA II, Clinical Research Associate, Belgium, Monitor, Monitoring, Senior Clinical Research Associate, CRA I, Field Based, CRO, Pharmaceutical, CRA

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