• Clinical Operations Professionals

    Astrix Technology (NJ)
    …Clinical Project Manager + Site Start Up Specialists + Clinical Data Manager + Clinical Development Associates + SAS Programmer + and more! We are an ... ** 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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  • Clinical Programmer , Integrated…

    J&J Family of Companies (Titusville, NJ)
    …Johnson Innovative Medicine is searching for the best talent for the position of ** Clinical Programmer ** to join our Integrated Data Analytics and Reporting team ... have multiple openings for this position. Position Summary: The Clinical Programmer is an individual contributor with...reporting. May include SAS , R, Python, etc. SAS knowledge is preferred for Clinical Programming… more
    J&J Family of Companies (09/17/25)
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  • Senior Scientist, Statistical Programmer…

    Merck (Rahway, NJ)
    …Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 5 years SAS programming experience in a clinical trial environment + MS in ... Applied Mathematics, Life Sciences, Engineering or related field plus 3 years SAS programming experience in a clinical trial environment **Department Required… more
    Merck (09/27/25)
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  • Statistical Programmer (Data & Statistical…

    AbbVie (Florham Park, NJ)
    …report clinical trial data under direction of Senior Statistical Analyst. + Provide SAS programming support for clinical trials. + Develop SAS programs ... of work experience in each of the following: + providing SAS programming support for pharmaceutical industry clinical trials; + coding SAS programs using … more
    AbbVie (09/18/25)
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  • Principal Statistical Programmer

    Regeneron Pharmaceuticals (Warren, NJ)
    A principal statistical programmer provides timely support to the study team on all programming matters according to the project strategies. As an integral part of a ... provides project leadership and programming support for processing data from clinical studies. Requirements will be identified according to a Statistical Analysis… more
    Regeneron Pharmaceuticals (07/31/25)
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  • Sr. Scientist, Statistical Programmer…

    Merck (Rahway, NJ)
    …Driving License:** No **Hazardous Material(s):** N/A **Required Skills:** CDISC ADaM, Clinical SAS Programming, Database Management Systems (DBMS), Data ... Life Sciences, Engineering or related field plus 5 years SAS programming experience in a clinical trial environment + MS in Computer Science, Statistics, Applied… more
    Merck (09/26/25)
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  • Associate Principal Scientist, Statistical…

    Merck (Rahway, NJ)
    …Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 9 years SAS programming experience in a clinical trial environment. + MS in ... Engineering or related field plus 7 or more years SAS programming experience in a clinical trial...more years SAS programming experience in a clinical trial environment. **Department Required Skills and Experience:** +… more
    Merck (09/30/25)
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  • Sr. Scientist, Statistical Programming- PKPD…

    Merck (Rahway, NJ)
    …Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 5-9 years SAS programming experience in a clinical trial environment + MS in ... Applied Mathematics, Life Sciences, Engineering or related field plus 3-7 years SAS programming experience in a clinical trial environment **Department Required… 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 ... as the quality control plan. + Perform and/or coordinate with study programmer the production of statistical analyses. Review and examine statistical data… 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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