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    Senior Statistical Programmer - London, United Kingdom - Lifelancer

    Lifelancer
    Lifelancer London, United Kingdom

    1 week ago

    Default job background
    Full time
    Description

    As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM ADaM) to support or lead one or more Phase I-IV clinical trials. This role can be performed as fully remote.
    How you will contribute:

    • Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy, utilizing SAS programming
    • Generating and validating analysis datasets/analysis files, and complex tables, listings, and figures ( TLFs)
    • Production and QC / validation programming
    • Generating complex ad-hoc reports utilizing raw data and analysis datasets
    • Applying strong understanding/experience of Efficacy analysis
    • Communicating with and/or responding to internal cross-functional teams and client for project specifications, status, issues or inquiries
    • Performing lead duties for assigned clinical study under principle programmers oversight
    • Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc.
    • Being adaptable and flexible when priorities change
    • Generating and validating Non-CDISC transformation datasets and analysis datasets
    • Proficient knowledge with SDTM/ADaM and TLFs. General expertise with Figures
    • Individuals should be able to start programs from scratch and have the ability to handle complicated domains and outputs related to the protocol and SAP.
    • They must demonstrate a good understanding of the endpoints and data collection, with the ability to read and write specifications related to the respective implementation guides.
    • R complex macro writing are a plus

    What you offer:

    • Bachelors degree in one of the following fields Statistics, Computer Science, Mathematics, etc.
    • At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical Biotech industry with a bachelors degree or equivalent. At least 6 years of related experience with a masters degree or above.
    • Study lead experience, preferably juggling multiple projects simultaneously.
    • Strong SAS data manipulation, analysis and reporting skills.
    • Strong QC / validation skills.
    • Good ad-hoc reporting skills.
    • Solid ADaM and complex TFL skills.
    • Proficiency in efficacy analysis and survival analysis
    • Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials data.
    • Submissions experience utilizing and other submission documents
    • Excellent analytical troubleshooting skills.
    • Ability to provide quality output and deliverables, in adherence with challenging timelines.
    • Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.

    Please use the below link for job application and quicker response.

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