Covance

  • Sr Clin Res Assoc

    Job Location(s) BR
    Job Number
    2018-20869
    Job Category
    Clinical Research Associate
    Position Type
    Full-Time
  • Job Overview

    Senior Clinical Research Associate (Sponsor Dedicated)

     

    Are you ready to make a truly rewarding career change?  In this unique CRA position you will work closely with an exciting Pharmaceutical client in the cutting edge area of Oncology!  As an experienced CRA you’ll be involved in initiation, routine & close out visits.  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 work place, 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.

     

     

    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 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

     

    Preferred:

    • Thorough knowledge of Covance SOPs regarding site monitoring

    Experience

    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 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

     

    Preferred:

    • One (1) or more year’s additional experience in a related field (i.e. medical, clinical, pharmaceutical, laboratory, research, data analysis, data management or technical writing) is preferred
    • Local project coordination and/or project management

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