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  • Posted: Nov 26, 2023
    Deadline: Not specified
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    Cytel Inc., an advanced analytics leader with over thirty years of experience providing sophisticated quantitative insights to executive decision-makers in the lifesciences. Cytel employs a range of data science tools from biostatistics to machine learning to help executives in the life-sciences to make confident decisions powered by data. We are probably...
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    Senior/Principal Statistical Programmer - Remote

    How you will contribute:

    • Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming
    • Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures ( TLFs)
    • Production and QC / validation programming
    • Generating complex ad-hoc reports utilizing raw data
    • Applying strong understanding/experience of Efficacy analysis
    • Creating and reviewing submission documents and eCRTs
    • Communicating with and/or responding to internal cross-functional teams and client for project specifications, status, issues or inquiries
    • Performing lead duties when called upon
    • 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

    To be successful in this position you will have:

    • Bachelor’s 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 bachelor’s degree or equivalent.
    •  At least 6 years of related experience with a master’s degree or above.
    • Study lead experience, preferably juggling multiple projects simultaneously preferred.
    • Strong SAS data manipulation, analysis and reporting skills.
    • Solid experience implementing the latest CDISC SDTM / ADaM standards.
    • Strong QC / validation skills.
    • Good ad-hoc reporting skills.
    • Proficiency in Efficacy analysis.
    • Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials’ data.
    • Submissions experience utilizing define.xml and other submission documents.
    • Experience supporting Rare diseases and Gastro Intestinal studies would be a plus.
    • 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.

    Method of Application

    Interested and qualified? Go to Cytel on careers.cytel.com to apply

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