PRAHS

  • Clinical Data Scientist

    Job Locations - | United Kingdom | United Kingdom-Reading | United Kingdom-Swansea
    Posted Date 1 week ago(5/14/2018 5:43 AM)
    ID
    2018-46743
  • Overview

    Clinical Data Scientist

     

    Location: UK, office-based in Swansea OR Reading

     

    At PRA, we don’t make our 15000+ people great. It’s the other way around. As we have grown to a top-5 CRO, we have maintained the feel of a small company, dedicated to collaboration and passion for what we do.

     

    We always have a desire to keep seeking new and better ways to operate. We don’t settle for the same old ways. Our passion for improving patient lives worldwide permeates all that we do. Put simply, we care.

     

    Responsibilities

    Due to growth we are currently seeking a Clinical Data Scientist, to work as part of an established global group that supports project teams in analyzing clinical data to identify risks and data issues, using advanced analytical techniques.

     

    Acting as a Key Functional Lead on projects; the Clinical Data Scientist will assess trial compliance, perform trending analysis, exploratory data reviews and report findings to internal and external stakeholders.

     

    Key responsibilities in this role include:

     

    • Developing and maintaining study documents specifying strategy, approach and procedures on assigned protocols/projects.
    • Providing input to applications, databases and systems used to assess study data quality.
    • Reviewing clinical data at aggregate level regularly throughout assigned studies using analytical reporting tools to support the identification of risks and data patterns/trends.
    • Creating analytical reports and presentations to facilitate review and data-driven decision making during team meetings

    Qualifications

    You are:

     

    Analytically-minded, a problem-solver

    Here at PRA we want our employees to succeed and ensure that they are set up for this success through constant training, development and support. To enable success in this position you will have:

    • Bachelor’s degree (or equivalent) in a Scientific or Healthcare discipline
    • Previous experience, ideally in a similar role, but we are also open to considering people with other relevant clinical trials experience, including those working as Lead Data Managers, Programmers, Clinical Research Associates, Clinical Team Managers and Project Managers.
    • Familiarity with risk-based monitoring
    • Skills in aggregating data review and interpretation using visualization/analysis software e.g. JReview, Tableau, SAS

     

    You will be frequently collaborating within multi-cultural global teams, so will need to demonstrate excellent written and oral communication skills, exhibit pro-active teamwork alongside a positive attitude, and maintain up-to-date industry awareness and understanding of regulation/standards.

     

    Your health, your family, your career, your money — the things that matter to you, matter to us. The benefits of PRA just get better and better.

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