Covance

  • Clin Res Assoc II

    Job Location(s) FR-Rueil-Malmaison
    Job Number
    2018-25804
    Job Category
    Clinical Research Associate
    Position Type
    Full-Time
  • Job Overview

    Covance is recruiting a CRA level II or III  to reinforce our team in France!

     

    This is a Sponsor dedicated position which will allow you initially to monitor sites in various countries in Europe: UK, France, Belgium, Czech Republic) for about 12 months before integrating fully our dedicated monitoring team in France. 

     

    You will be part of a supportive team and involved in challenging projects, performing remote and on-site monitoring visits. 

     

    Seize the chance to be part of some of the most innovative projects of the industry! 

     

    Responsibilities: 

    • International monitoring of registry studies in Rare Disease in France, Belgium, UK and Czech Republic) for about 6 months. You will be then involved in monitoring studies in France only. 
    • Prepare accurate and timely trip reports
    • Independently perform CRF review; query generation and resolution against established data review guidelines on Covance or client data management systems as assigned by management
    • Assist with training, mentoring, and development of new employees, e.g. co-monitoring
    • Co-ordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable), and may act as a local client contact as assigned
    • Perform other duties as assigned by management

    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)
    • 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
    • Excellent level of English, both written and spoken as you will be liaising with site staff in English 

    Experience

    You have gained already some valuable experience in clincical research as a CRA within a CRO or pharma environment and are looking to join a dynamic working environment investing in their employees' potential and career development. 

     

    Apply now for this role and/or contact directly gerda.quenum@covance.com 

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