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Maidenhead

    Lead Senior Programmer - Maidenhead, Berkshire, United Kingdom - Fortrea

    Fortrea
    Fortrea Maidenhead, Berkshire, United Kingdom

    5 days ago

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    Description

    As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas.

    As a Lead Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit, you are central to the successful delivery of complex oncology projects for a renowned, innovative and global top pharmaceutical company.

    You will be involved in liaising with the entire study team as needed, including Clinical, Medical Writing, Safety and Biometrics.

    It is a great opportunity to see more how this works from a Big Pharma perspective, whilst still being part of a global CRO with opportunity for future career growth.

    Stand at the forefront of Oncology research.

    You can be 100% home-based in EMEA or, if you prefer, you can work from our local office in your home country.

    Highly competitive compensation packages, including various local benefits such as pension contributions, complimentary health insurance plans, remote working allowances etc.

    A genuine work life balance
    A permanent employment contract with Fortrea
    Excellent training and career development opportunities, as well as support with advancing your individual education
    Strong support from your Line Manager and your team, as well as from more than 20,000 Fortrea colleagues worldwide

    Plan, execute and oversee all programming activities on a study, including but not limited to: resource estimation, working within budget, meeting timelines, maximizing quality, interaction with other departments, etc.

    Oversee SDTM, ADaM and TLF development, perform Senior Review of outputs
    Liaise with other Sponsor departments for additional programming needs, as required to support publications, medical writing and additional development needs and analyses
    Ensure all activities are conducted efficiently, with appropriate set-up of needed tools and macros, prioritizing quality at all times
    Ideally, a degree in a relevant field such as mathematics, life sciences, statistics, computer sciences, etc.
    In lieu of the above: professional experience in statistical programming within clinical trials in a biotech, CRO or pharmaceutical company
    Solid experience with complex oncology clinical trials (minimum 5 years) and the corresponding datasets' content (safety and efficacy) and endpoints
    Lead experience in Oncology trials (from pharma or CRO perspective)
    Biostatistics and Clinical Data Management
    Expert knowledge of base SAS, SAS macros, SAS/STAT and in debugging SAS programs
    xml, Reviewer's Guides and submission standards
    Fluency in English - both verbal and written - is a must


    REMOTE
    #Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. For more information about how we collect and store your personal data, please see our Privacy Statement . #
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