• Clinical Programmer , Integrated…

    J&J Family of Companies (Titusville, NJ)
    …Medicine is searching for the best talent for the position of ** Clinical Programmer ** to join our Integrated Data Analytics and Reporting team (IDAR). This ... NJ or Raritan, NJ. We have multiple openings for this position. Position Summary: The Clinical Programmer is an individual contributor with knowledge of data more
    J&J Family of Companies (09/17/25)
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  • Principal Statistical Programmer

    Regeneron Pharmaceuticals (Warren, NJ)
    …study, the incumbent provides project leadership and programming support for processing data from clinical studies. Requirements will be identified according to ... A principal statistical programmer provides timely support to the study team...with 3+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical… more
    Regeneron Pharmaceuticals (07/31/25)
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  • Senior Scientist, Statistical Programmer

    Merck (Rahway, NJ)
    …level **Position Specific Required Skills and Experience:** + Programming expertise with clinical endpoint data (efficacy and safety) and pharmacokinetic data ... in CDISC SDTM and ADaM standards + Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH + Designs… more
    Merck (09/27/25)
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  • Statistical Programmer ( Data

    AbbVie (Florham Park, NJ)
    …team member in R & D of new pharmaceutical products. + Analyze & report clinical trial data under direction of Senior Statistical Analyst. + Provide SAS ... programming support for clinical trials. + Develop SAS programs for creation of Analyst Data Models (ADaM), data sets following CDISC standards for either… more
    AbbVie (09/18/25)
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  • Associate Principal Scientist, Statistical…

    Merck (Rahway, NJ)
    …be programmed, an understanding of statistical terminology and concepts. + Familiarity with clinical data management concepts + Experience in CDISC and ADaM ... Specific Required Skills and Experience:** + Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH;… more
    Merck (09/30/25)
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  • Sr. Scientist, Statistical Programmer

    Merck (Rahway, NJ)
    …be programmed; an understanding of statistical terminology and concepts + Familiarity with clinical data management concepts + Experience in CDISC and ADaM ... Specific Required Skills and Experience:** + Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH;… more
    Merck (09/26/25)
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  • Clinical Operations Professionals

    Astrix Technology (NJ)
    …Manager + Site Start Up Specialists + Clinical Data Manager + Clinical Development Associates + SAS Programmer + and more! We are an equal opportunity ... ** Clinical Operations Professionals** Clinical Remote, NJ, US Pay Rate Low: 25 | Pay Rate High: 80 + Added - 06/02/2025 Apply for Job Astrix has been partnered… more
    Astrix Technology (08/08/25)
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  • Sr. Scientist, Statistical Programming- PKPD…

    Merck (Rahway, NJ)
    …datasets, and develop tables and figures according to the modeling analysis plans. The programmer will take on a data stewardship leadership role and be ... the creation of modeling data from original data source(s) to final modeling dataset. The programmer...Skills and Experience:** + Significant expertise in SAS and clinical trial programming including data steps, procedures,… more
    Merck (09/22/25)
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  • Associate Statistical Project Leader

    Sanofi Group (Morristown, NJ)
    …**Main Responsibilities:** + Provide high quality input into the design of the clinical study (including protocol development), the setup and conduct of the study to ... make sure data are adequately captured and collected to answer the...quality control plan. + Perform and/or coordinate with study programmer the production of statistical analyses. Review and examine… more
    Sanofi Group (09/09/25)
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  • Associate Statistical Project Leader

    Sanofi Group (Morristown, NJ)
    …started? **Main Responsibilities** + Provide high quality input into the design of the clinical study, the setup and conduct of the study + Accountable for all ... according to the statistical analysis plan: perform and/or coordinate with study programmer the production of statistical analyses + Prepare statistical methods &… more
    Sanofi Group (09/19/25)
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