• Merck & Co. (Rahway, NJ)
    …and develop tables and figures according to statistical/modeling analysis plan. The senior programmer will partner with stakeholders to solve problems; reduce ... increase in efficiency and compliance for statistical/modeling analyses. -The senior programmer will also write programs to...Life Sciences, Engineering or related field plus 5-9 years SAS programming experience in a clinical trial… more
    HireLifeScience (07/31/25)
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  • Merck & Co. (North Wales, PA)
    …Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 5-9 years SAS programming experience in a clinical trial environment MS in ... Life Sciences, Engineering or related field plus 3-7 years SAS programming experience in a clinical trial...3-7 years SAS programming experience in a clinical trial environment - Department Required Skills and Experience:… more
    HireLifeScience (05/21/25)
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  • Merck & Co. (Rahway, NJ)
    …for the benefit of patients and global human health.Responsibilities: The Senior Statistical Programmer , Submission Data Standards Quality Management (SDS ... Life Sciences, Engineering or related field plus 5 years SAS programming experience in a clinical trial...5 years SAS programming experience in a clinical trial environmentMS in Computer Science, Statistics, Applied Mathematics,… more
    HireLifeScience (07/29/25)
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  • Merck & Co. (Rahway, NJ)
    …execute statistical analysis and reporting deliverables under the guidance of a senior -level programmer supporting early-phase oncology clinical trials. ... Engineering or related field plus at least 2 years SAS programming experience in a clinical trial...and complete programming tasks under the guidance of a senior programmer at a project level; and… more
    HireLifeScience (06/18/25)
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  • Merck & Co. (Rahway, NJ)
    …to take direction effectively and complete programming tasks under the guidance of a senior programmer at a project level; and to collaborate with key ... figures and submission deliverables under the guidance of a senior level programmer .Perform validation tasks according to...Engineering or related field plus at least 2 years SAS programming experience in a clinical trial… more
    HireLifeScience (06/17/25)
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  • Senior SAS Research…

    University of Southern California (Los Angeles, CA)
    Senior SAS Research Programmer - USC Schaeffer CenterApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA University-Park-Campus/ ... health behavior research and related health policy topics. The Senior SAS Research Programmer will...uniquely spans the entire spectrum of pharmaceutical development and clinical care - from drug discovery to regulatory approaches… more
    University of Southern California (05/17/25)
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  • Senior Statistical Programmer

    Merck (North Wales, PA)
    …and develop tables and figures according to statistical/modeling analysis plan. The senior programmer will partner with stakeholders to solve problems; reduce ... increase in efficiency and compliance for statistical/modeling analyses. The senior programmer will also write programs to...Life Sciences, Engineering or related field plus 5-9 years SAS programming experience in a clinical trial… more
    Merck (07/31/25)
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  • Senior Statistical Programmer FSP

    Cytel (Boise, ID)
    …part of this new program. **Position Overview:** As a Senior Statistical Programmer , you will leverage your advanced SAS programming skills and proficiency ... at the heart of our client's innovation. As a Senior Statistical Programmer you will be dedicated...Science, Mathematics, etc. + At least 8 years of SAS programming working with clinical trial data… more
    Cytel (07/24/25)
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  • Senior Statistical Programmer FSP…

    Cytel (Tallahassee, FL)
    …part of this new program. **Position Overview:** As a Senior Statistical Programmer , you will leverage your advanced SAS programming skills and proficiency ... at the heart of our client's innovation. As a Senior Statistical Programmer you will be dedicated...Science, Mathematics, etc. + At least 7 years of SAS programming working with clinical trial data… more
    Cytel (07/19/25)
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  • Senior Statistical Programmer , Late…

    Merck (North Wales, PA)
    …Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 5-9 years SAS programming experience in a clinical trial environment + MS in ... Life Sciences, Engineering or related field plus 3-7 years SAS programming experience in a clinical trial...3-7 years SAS programming experience in a clinical trial environment **Department Required Skills and Experience:** +… more
    Merck (05/21/25)
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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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  • Senior Manager, Statistical Programming…

    Ascendis Pharma (Palo Alto, CA)
    …at least 7 years of relevant experience. + Proven experience as a lead programmer for clinical trials and complex technical projects. + Excellent knowledge of ... for employees to grow and develop their skills. The Senior Manager, Statistical Programming, will be expected to provide...expected to provide timely and strategic programming support to clinical study teams in alignment with project goals. This… more
    Ascendis Pharma (07/11/25)
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  • Scientist, Statistical Programming

    Merck (Rahway, NJ)
    …execute statistical analysis and reporting deliverables under the guidance of a senior -level programmer supporting early-phase oncology clinical trials. ... Engineering or related field plus at least 2 years SAS programming experience in a clinical trial...and complete programming tasks under the guidance of a senior programmer at a project level; and… more
    Merck (06/18/25)
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  • Scientist, Statistical Programming

    Merck (Rahway, NJ)
    …to take direction effectively and complete programming tasks under the guidance of a senior programmer at a project level; and to collaborate with key ... figures and submission deliverables under the guidance of a senior level programmer . + Perform validation tasks...Engineering or related field plus at least 2 years SAS programming experience in a clinical trial… more
    Merck (06/17/25)
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  • Sr. Scientist, Statistical Programming- SDTM,…

    Merck (North Wales, PA)
    …for the benefit of patients and global human health. **Responsibilities:** The Senior Statistical Programmer , Submission Data Standards Quality Management (SDS ... 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 (07/29/25)
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  • Data Analyst

    University of Michigan (Ann Arbor, MI)
    …programming, analysis and reporting using large administrative claims and clinical extracts. **Mission Statement** Michigan Medicine improves the health of ... position involves a wide range of tasks including claims and clinical data management, provider participation and performance tracking for value-based reimbursement… more
    University of Michigan (07/31/25)
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  • Biostatistical Analyst II (Remote Capable)

    Geisinger (Danville, PA)
    …needed to provide statistical support to clinical investigators. + Experienced SAS or R programmer for both data manipulation and statistical analysis. ... master's-level biostatistician. Responsibilities include collaborating on the design of clinical research studies, writing biostatistical analysis plans for research… more
    Geisinger (06/01/25)
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  • Biostatistician (Remote Capable)

    Geisinger (Danville, PA)
    …needed to provide statistical support to clinical investigators. + Experienced SAS or R programmer for both data manipulation and statistical analysis. ... doctorate-level biostatistician. Responsibilities include collaborating on the design of clinical research studies, writing biostatistical analysis plans for research… more
    Geisinger (06/01/25)
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