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    Project Statistician - United Kingdom - Warman O'Brien

    Warman O'Brien
    Warman O'Brien United Kingdom

    2 weeks ago

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    Description
    Principal Biostatistician – Leading CRO – Homebased – UK / Europe

    We have recently partnered with an award winning CRO, who are looking for an experienced Principal Statistician (or Senior looking to move into Principal), to join their successful study delivery team, any area of specialism considered, Oncology also advantageous.


    Also responsible for planning, monitoring, organizing and reviewing activities of biostatisticians and programmers working on the assigned program of studies, ensuring individual studies and the overall program of studies and integrated analyses are delivered on time, on budget to required quality.

    Review project database structures, edit checks and data management coding conventions
    Preparation of statistical analysis plans including the definition of derived data, and the design of statistical tables, figures, and data listings for clinical summary reports
    Statistical analysis, Interpretation of data and reporting of results
    Writing of the statistical methods sections of integrated study reports. Supports responses to regulatory questions on the design of the program, and any labelling claims following submission

    Preparation of biostatistics input to company research proposals and participates in proposal defense meetings and makes presentations at marketing meetings with prospective client.

    D. degree in statistics, biostatistics, or related field.
    Experience in statistics, biostatistics or related field
    Review project database structures, edit checks and data management coding conventions
    Preparation of statistical analysis plans including the definition of derived data, and the design of statistical tables, figures, and data listings for clinical summary reports
    Statistical analysis, Interpretation of data and reporting of results.
    Writing of the statistical methods sections of integrated study reports. Experience leading a regulatory submission
    Supports responses to regulatory questions on the design of the program, and any labelling claims following submission

    Preparation of biostatistics input to ICON research proposals, and participates in proposal defense meetings and makes presentations at marketing meetings with prospective client.

    Knowledge of clinical trials methodology, regulatory requirements, statistics and statistical software packages, including SAS are a must.


    Ongoing development is vital, and as a Principal Biostatistician you will have the opportunity to progress your career, with the potential to move into other related areas to enhance your skill set.

    In comparison with their competitor's and pharmaceutical companies, they provide more flexible working platforms for coaching and educating newcomers to be highly respected professionals in our industry.

    The company like to look at themselves more like an extended family with consideration of staff as individuals allowing a work-life balance.


    Company culture:


    Diverse teams enable them to become a better partner to their customers and help to fulfil our mission to advance and improve patients' lives.

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