• Biostatistician 2

    Job Locations - | United Kingdom-Reading
    Posted Date 9 months ago(9/28/2017 9:12 AM)
  • Overview

    PRA Health Sciences is an award winning CRO.


    We are proud to have won Pharma Times 'Clinical Research Company of the Year' in 2017 for the fourth consecutive year. We aren’t winning these awards by chance; PRA is being recognised industry-wide for our dedication to the future of clinical development. Most importantly for you, at PRA we recognise that our success is down to our people.


    Position overview:


    PRA's European Biostatistics team has some exciting growth plans for 2018, therefore we are looking for experienced Biostatisticians to join our team.


    The Biostatistics team are consistently focussed on identifying and retaining industry leading talent. Using a supportive and engaged management style they will provide a focus for staff development alongside an effective work/life balance.


    Biostatistician role summary:

    • Provide statistical oversight across clinical trials in all phases and in a wide variety of therapeutic areas.
    • Design, plan and execute Biostatistical components of clinical trials including writing Statistical Analysis Plans (SAP) and inferential analysis programming.
    • Functional lead for the statistics and programming portion of the study including accountability for timelines, budget and resourcing of the study
    • Mentoring junior Biostatisticians through our structured graduate training programme.


    You are:


    MSc qualified Statistician, project delivery focused and have excellent communication skills

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

    • MSc or PhD in Medical Statistics with solid experience working within a CRO and or the pharmaceutical industry
    • Excellent statistical and communication skills
    • The ability to contribute your statistical expertise to the design, analysis and reporting of global clinical studies
    • The ability to plan, supervise, implement, and monitor the statistical processes for your complex clinical trials.
    • Ability to successfully interact with your sponsors when leading your complex projects.


    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.


    PRA Health Sciences is an Equal Opportunity Employer. We welcome and encourage diversity in the workplace.


    For more information please visit our website:



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