Covance

  • Sr Clin Res Assoc

    Job Location(s) BR
    Job Number
    2018-20613
    Job Category
    Clinical Research Associate
    Position Type
    Full-Time
  • Job Overview

    See what Covance CRAs have to say

    “I work very hard but have a good balance. My manager is very supportive and in tune to my professional development.”

    "I have really enjoyed working with my colleagues to accomplish project objectives and can see that what I do has an impact on the success of this company."

    "Clients want to work with us. I truly believe we have quality work and quality people.”

    The CRA opportunity

    Beyond the excellent compensation and comprehensive benefit package you'll receive as a Clinical Research Associate, joining Covance opens the door to many career opportunities. Learn more about what’s possible with a company who truly invests in you at http://covance.com/CRAcareers.

    Get to know Covance

    At Covance, we value your unique point of view and bold ideas to help bring innovative medicines to market and advance modern healthcare. Join our supportive team and see how our flexible work environment along with mentoring, training and career development can help you thrive personally and professionally.

    Together, let’s shape new possibilities for your career and improve the lives of patients around the world.

    Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran/Sexual Orientation/Gender Identity).

    Your confidentiality and privacy are important to us.

    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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