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    SAS Data Programmer - United Kingdom - PHASTAR

    PHASTAR
    Default job background
    Part time
    Description

    Phastar is a multiple award-winning global biometric Contract Research Organization (CRO) that is accredited as an outstanding company to work for by Best Companies.

    We partner with pharmaceutical, biotechnology and medical device organizations to provide the expertise and processes to manage and deliver on time, quality biostatistics, programming, data management and data science services.

    Our unique approach to data analysis, "The Phastar Discipline", has led us to build a reputation for outstanding quality.

    With this as our core focus, we're looking for talented individuals who share our passion for quality and technical expertise to join our team.

    Accredited as an outstanding company to work for, Phastar is committed to employee engagement, workplace satisfaction and ensuring a healthy work-life balance.

    We offer flexible working, part-time hours, involvement in developing company-wide initiatives, structured training and development plans, and a truly supportive, fun and friendly environment.

    What's more, when you join our team, Phastar will plant a tree in your honour, as one of our Environmental, Social and Governance (ESG) initiatives.

    So, not only would you get your dream job, you'll also be helping to save the planet
    producing non-complex datasets and outputs to excellent quality whilst adhering to deliverable timelines.

    Awareness of CDISC SDTM and ADaM implementation guidelines; reviewing and updating non-efficacy/non-complex data specifications; understanding Statistical Analysis Plans (SAPs) and output shells for day to day programming activities.

    Excellent team work ethos, willingness to help others and learn new skills from working in a team environment.

    This position is remote (although can be office based or hybrid, depending on your location) and will involve occasional travel to events throughout the year.

    Create, QC and update simple, non-efficacy dataset specifications for single studies
    Review simple study design SAP with supervision
    Awareness of CDISC SDTM and ADaM implementation guidelines
    Educated to degree or diploma level (or equivalent) within Maths, Computer Science or a related discipline
    Experience of SAS Programming

    With the world's eyes focused on clinical trial data, this is a fantastic time to join an award-winning specialized biometric CRO that is renowned for its technical expertise, outstanding quality and cutting-edge data science techniques.

    We offer flexible working, part-time hours, structured training and development plans, continuous learning opportunities, and a competitive salary and benefits package.

    We're committed to ensuring our employees achieve a healthy work-life balance, within a supportive, fun and friendly working environment.

    Please note that we are considering candidates located anywhere in the UK as this role can be carried out remotely.

    It is our policy to employ individuals on the basis of their suitability for the work to be performed and their potential for development, regardless of age, sex, race, colour, nationality, ethnic or national origin, disability, marital status, pregnancy or maternity, sexual orientation, gender reassignment, religion, or belief.



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