• Principal Statistical Programmer

    IQVIA (Trenton, NJ)
    …database components and theory. + Excellent application development skills. + Strong understanding of clinical trial data and extremely hands on in data ... client requirements. **Job Details:** + Position: - Principal Statistical Programmer + Home Based + Min 7+ years of...Must have expertise of R programming as well as SAS (R) Base, and good knowledge of SAS (R)… more
    IQVIA (06/19/25)
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  • Senior Statistical Programmer FSP

    Cytel (Trenton, NJ)
    …Performing data manipulation, analysis and reporting of clinical trial data , both safety and efficacy (ISS/ISE), utilizing SAS programming + Production ... this new program. **Position Overview:** As a Senior Statistical Programmer , you will leverage your advanced SAS ...8 years of SAS programming working with clinical trial data in the Pharmaceutical &… more
    Cytel (04/25/25)
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  • Principal Statistical Programmer

    Regeneron Pharmaceuticals (Basking Ridge, 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 (04/16/25)
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  • Associate Principal Scientist, Statistical…

    Merck (Rahway, NJ)
    …Specific Required Skills and Experience:** + Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS /MACRO, ... Life Sciences, Engineering or related field plus 9 years SAS programming experience in a clinical trial...understanding of statistical terminology and concepts. + Familiarity with clinical data management concepts + Experience in… more
    Merck (05/28/25)
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  • Senior Statistical Programmer

    Regeneron Pharmaceuticals (Basking Ridge, NJ)
    …or related discipline with 3+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related ... JOB RESPONSIBILITIES: * Support and/or lead programmer for programming and QC of analysis datasets,...analysis datasets, TFLs or standard tools following Regeneron standard data models or user requirements. Assist in the coordination… more
    Regeneron Pharmaceuticals (04/01/25)
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  • Principal Statistical Programmer FSP - RWD

    Cytel (Trenton, NJ)
    …(Clinformatics Datamart(R) and Market Clarity), Truveta and UK Biobank. Experience analyzing clinical trial and/or registry data is desirable. + Familiarity with ... by:** + Providing support to the Epidemiology team by preparing Real World data , advising on data analytic strategies, and supporting stakeholders in various… more
    Cytel (06/17/25)
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  • Sr. Scientist, Statistical Programming- PKPD…

    Merck (Rahway, NJ)
    …Specific Required Skills and Experience:** + Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS /MACRO, ... and figures according to the modeling analysis plans. The programmer will take on a data stewardship...Life Sciences, Engineering or related field plus 5-9 years SAS programming experience in a clinical trial… more
    Merck (06/24/25)
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  • Clinical Operations Professionals

    Astrix Technology (NJ)
    … Project Manager + Site Start Up Specialists + Clinical Data Manager + Clinical Development Associates + SAS Programmer + and more! We are an equal ... ** 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 (05/09/25)
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  • Scientist, Statistical Programming

    Merck (Rahway, NJ)
    …requests, clinical study reports, and new drug application filing. Produce SAS data transport files and program text files for regulatory submission. ... analysis and reporting deliverables under the guidance of a senior-level programmer supporting early-phase oncology clinical trials. Collaborate with other… more
    Merck (06/18/25)
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  • Scientist, Statistical Programming

    Merck (Rahway, NJ)
    …Mathematics, Life Sciences, Engineering or related field plus at least 2 years SAS programming experience in a clinical trial environment. **Required experience ... submission deliverables under the guidance of a senior level programmer . + Perform validation tasks according to departmental SOPs...and skills** + Must possess SAS programming skills including data… more
    Merck (06/17/25)
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