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Clinical SAS Programmer

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Katalyst HealthCares & Life Sciences
📍 Edison, United States
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Location Edison
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Posted June 12, 2026
🚗
Commute Local Area
🎯
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Job Description


Responsibilities:
  • Effectively manage and oversee statistical programming resources including contractors and CROs related to statistical programming deliverables to ensure high-quality within timeline and budget.

  • Conduct hands-on validation/QC of CRO deliverables to ensure high-quality (SDTMs, ADaMs, TFLs) and ensure accuracy of clinical trial results for internal and external audiences.

  • Ensure all relevant deliverables including investigator brochures, publications, all regulatory submissions (SDTM/ADaM compliance), supporting documentation (, reviewer's guide, annotated CRFs) conforms to SOPs and to regulatory specifications.

  • Conduct hands-on programming of deliverables including but not limited to IDMC meetings, DSUR, IB safety data review, Board meetings, Exploratory Analysis, etc.

  • Ensure timely delivery of all statistical deliverables for each study assigned.

  • Collaborate with study statisticia...

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    📍 Location Details

    🌆
    City
    Edison
    🗺️
    Country
    United States
    🚗
    Commute
    Local Area

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