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Somerset

    Senior Analyst/Programmer - Somerset, United States - Katalyst Healthcares and Life Sciences

    Katalyst Healthcares and Life Sciences
    Katalyst Healthcares and Life Sciences Somerset, United States

    2 weeks ago

    Default job background
    Description
    Responsibilities:
    • Overseeing SAS programming activities from varying aspects: programming, statistical and clinical
    • Create, manage, and maintain the SAS programming algorithm for the clinical study database and data analysis
    • Peer review the submission packages and contribute to the input of SAP and mock TFLs
    • Perform ad hoc analyses to support Phase I to IV clinical trials and medical publications
    • Maintain relationships with internal and external customers and vendors
    • Mentor up and coming junior programmers and analysts
    • Tracking projects against goals and submit status reports to project management
    Requirements:
    • Bachelor's or advanced degree in statistics, biostatistics, computer science or related fields
    • 4 to 6 years' experience in the pharma/biotech industry
    • dvanced SAS programming skills (e.g, SAS SQL, SAS Macro, SAS/STAT, SAS/GRAPH, etc.) with clinical trial data
    • dvanced knowledge in industry standards, such as the ICH guidelines, CDISC standards, 21 CFR Part 11, and FDA guidelines
    • Experience in handling and processing upstream data, e.g., EDC, eDT, SDTM, and in providing outputs to meet downstream requirements, e.g., ADaM, and TFLs
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