Covance

  • Sr Clin Res Assoc

    Job Location(s) FR-Paris
    Job Number
    2018-24303
    Job Category
    Clinical Research Associate
    Position Type
    Full-Time
  • Job Overview

    Covance is recruiting an experienced CRA to be dedicated to a very innovative biotech. This role is office-based in the paris area, North of France or Nantes. This is a great opportunity to join our organisation and to be part of a very dynamic and motivationf work environment. 

     

    This is time to join our EMEA FSPx Team! 

    Education / Qualifications

    • External Candidates
      • University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure),

    AND

      • a minimum of 4 years of Clinical Monitoring experience
      • In lieu of the above education requirement, external candidates with a minimum of 6 years recent clinical monitoring experience will be considered
    • Internal Candidates
      • Internal candidates with a minimum of 4 years of clinical monitoring experience.
    • Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements in other countries
    • Thorough understanding of the drug development process
    • Fluent in local office language and in English, both written and verbal

    Experience

    • External Candidates
      • University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure),

    AND

      • a minimum of 4 years of Clinical Monitoring experience
    • In lieu of the above education requirement, external candidates with a minimum of 6 years recent clinical monitoring experience will be considered.
    • Internal Candidates
      • Internal candidates with a minimum of 4 years of clinical monitoring experience.
    • Have a full understanding of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
    • Advanced site monitoring skills
    • Advanced study site management skills
    • Advanced registry administration skills
    • Ability to work with minimal supervision
    • Good planning and organization skills
    • Good computer skills with good working knowledge of a range of computer packages
    • Advanced verbal and written communication skills
    • Ability to train and supervise junior staff
    • Ability to resolve project-related problems and prioritizes workload for self and team
    • Ability to work within a project team
    • Works efficiently and effectively in a matrix environment

    Options

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