Covance

  • Clin Res Assoc I

    Job Location(s) AR-Buenos Aires
    Job Number
    2019-27108
    Job Category
    Hidden (54284)
    Position Type
    Full-Time
  • Job Overview

    Are you an organized person who can work independently and take ownership of your career? Would you like to gain on-the-job skills while helping advance life-changing medicines?

    If you are looking to enter a nurturing environment that provides a clear path to advancement, consider furthering your career as a Covance Clinical Research Associate (CRA). In this role, you will:

    • Support large, prominent pharmaceutical companies with their clinical trials
    • Oversee site monitoring responsibilities with remote and in-person visits
    • Work in a flexible environment with a close-knit team
    • Use time management and people skills to ensure compliance

    Education/Qualifications

    Minimum Required:

    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 six months on-site monitoring (preferred).

     

     Internal candidates

    -Internal candidates with a minimum of 6 months of experience as a Clinical Research Assistant

    or

    -Internal candidates with a minimum 2 years clinical trials or site management experience (e.g. study coordinator, project coordinator, project specialist, study start- up)

     

    -Basic understanding of ICH Guidelines and GCP including a basic understanding of regulatory requirements

    -Basic understanding of the clinical trial process

    -Valid Driver’s License

    Preferred:

    Working knowledge of Covance SOPs for site monitoring

     

    Experience

    Minimum Required:

    • External Candidates

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

     

    AND

    o  a minimum of six months of on-site monitoring (preferred)

     

    • Internal candidates

    o    Internal candidates with a minimum of 6 months of experience as a Clinical Research Assistant

     

    OR

     

    o  Internal candidates with a minimum 2 years clinical trials or site management experience (e.g. study coordinator, project coordinator, project specialist, study start-up)

    • Ability to monitor study sites according to protocol monitoring guidelines, SOPs, ICH Guidelines and GCP
    • Ability to work within a project team
    • Good planning, organization and problem solving abilities
    • Good communication skills, oral and written
    • Good computer skills
    • Works efficiently and effectively in a matrix environment
    • Fluent in local office language and in English, both written and verbal

     

    Preferred:

    • One (1) or more additional years of experience in a related field (i.e., medical, clinical, pharmaceutical laboratory, research, data analysis, data management or technical writing) is preferred

     

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