Covance

  • Clin Res Assoc II

    Job Location(s) PE-Lima
    Job Number
    2018-26223
    Job Category
    Clinical Research Associate
    Position Type
    Full-Time
  • Job Overview

    Are you ready to redefine what’s possible, and discover your extraordinary potential at Covance? A career here provides the unique chance to create a lasting impact and difference in our patient’s lives. Joining our team will offer you a rewarding career, an opportunity to work in a high-energy & collaborative workplace, along with access to comprehensive benefits. Your work will be meaningful, the patient outcomes are real, and the results are lasting. With the support of exceptional people from across the globe and an energized purpose, you’ll be empowered to own your career journey with mentoring, training and personalized development planning.

    Our mission is to help our clients bring the miracles of medicine to market sooner -- join us for your next career move.

    Education/Qualifications

    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 2 years of Clinical Monitoring experience.
     Internal Candidates
    o Internal candidates with a minimum of 2 years of Clinical Monitoring experience
     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
    Preferred:
     Thorough 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 2 years of Clinical Monitoring experience.
     Internal Candidates
    o Internal candidates with a minimum of 2 years of Clinical Monitoring 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
    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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