• Clinical Data Coordinator II

    Job Location(s) UK-Maidenhead
    Job Number
    Job Category
    Clinical Data Management
    Position Type
  • Job Overview

    Get ready to redefine what’s possible and discover your potential at Covance. Here, you’ll have the opportunity to personally advance healthcare and make a difference in peoples’ lives with your ideas and rare point of view. 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.


    Are you looking for a stable position with a well-established company, a place where you could feel comfortable? Do you like working with people who are friendly and reliable? Join us as we speed the delivery of groundbreaking therapies and anticipate tomorrow’s drug development challenges, building new possibilities for our clients.


    Location: office-based Maidenhead, United Kingdom


    Role description:

    Serve as a member of the project team with primary responsibility for clinical data review, query generation / resolution and reconciliation activities to support the delivery of clinical data according to client quality and integrity specifications, and project timelines and productivity targets.

    Education / Qualifications

    Minimum Requirement:

    University / college degree (life science, pharmacy or related subject preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing certification, medical or laboratory technology).

      • In lieu of the above requirement, approximately 18 months experience in related field incorporating approximately one year’s clinical data management experience in addition to the two years relevant work experience in data management will be considered
      • Knowledge of drug development process
      • Knowledge of effective clinical data management practices
      • Knowledge of ICH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs
      • Fluent in English, both written and verbal


    Your experience:

    • Minimum two years’ relevant work experience with increasing responsibility in data management with knowledge of one or more therapeutic areas
    • Demonstrated time management skill and ability to adhere to project productivity metrics and timelines
    • Potential ability to lead by example data management staff
    • Demonstrated ability to work in a team environment and collaborate with peers
    • Demonstrated interpersonal skills
    • Good oral and written communication skills
    • Ability to demonstrate a constructive problem solving attitude while dealing with time management demands, incomplete information or unexpected events

    There is no better time to join us!


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