Covance

  • Clin Res Assoc I

    Job Location(s) MX-Mexico City
    Job Number
    2018-23614
    Job Category
    Clinical Research Associate
    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

    Required:

    • 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.
    •  Thorough understanding of the clinical trial process.

    Experience

    • Ability to monitor study sites independently according to protocol monitoring guidelines, S.O.P.s, 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

    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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