Covance

  • Sr Clin Res Assoc

    Job Location(s) MX-Mexico City
    Job Number
    2018-21742
    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

    Required:

    • University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution, nursing certification, medical or laboratory technology
    • In lieu of the above requirement, candidates with four (4) or more years of relevant clinical research experience in pharmaceutical or CRO industries will be considered
    • 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

    Required:

    • Minimum of four (4) years of clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits)
    • In lieu of the above requirements, candidates with > four (4) years supervisory experience in a health care setting and three (3) years clinical research experience in the pharmaceutical or CRO industries (including monitoring) may be considered
    • Have a full understanding of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
    • Excellent site monitoring skills
    • Excellent study site management skills
    • Excellent 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
    • Excellent 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:      

    • Oncology experience 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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