• Senior Statistical Programmer- Analysis…

    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 (11/07/25)
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  • Senior Scientist, Statistical Programmer- Hybrid

    Merck (North Wales, PA)
    …Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 5 years SAS programming experience in a clinical trial environment + MS in ... Life Sciences, Engineering or related field plus 3 years SAS programming experience in a clinical trial...3 years SAS programming experience in a clinical trial environment **Department Required Skills and Experience:** +… more
    Merck (11/07/25)
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  • Associate Principal Statistical Programmer, Early…

    Merck (North Wales, PA)
    …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 (11/19/25)
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  • Sr. Scientist, Statistical Programmer, Late Stage…

    Merck (North Wales, PA)
    …Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 5 years SAS programming experience in a clinical trial environment + MS in ... Life Sciences, Engineering or related field plus 3 years SAS programming experience in a clinical trial...3 years SAS programming experience in a clinical trial environment _Department Required Skills and Experience:_ +… more
    Merck (09/05/25)
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  • Associate Principal Scientist, Statistical…

    Merck (North Wales, PA)
    …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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  • Senior/Principal Statistical Programmer PK Data…

    Cytel (Harrisburg, PA)
    …following fields Statistics, Computer Science, Mathematics, etc. + At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical & ... a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM...to support or lead one or more Phase I-IV clinical trials. This role can be performed as fully… more
    Cytel (11/13/25)
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  • Biostatistical Analyst II (Remote Capable)

    Geisinger (Danville, PA)
    …+ Possesses the critical thinking skills needed to provide statistical support to clinical investigators. + Experienced SAS or R programmer for both data ... master's-level biostatistician. Responsibilities include collaborating on the design of clinical research studies, writing biostatistical analysis plans for research… more
    Geisinger (10/03/25)
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  • Senior Scientist, Statistical Programming

    Merck (North Wales, PA)
    …Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 5 years SAS programming experience in a clinical trial environment + OR a ... Life Sciences, Engineering or related field plus 3 years SAS programming experience in a clinical trial...3 years SAS programming experience in a clinical trial environment. **Requirements:** + Experience in US and/or… more
    Merck (10/23/25)
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  • Principal Statistical Programmer

    IQVIA (Philadelphia, PA)
    …// IDV // EDCP **Key Skills:** + Must have expertise of R programming as well as SAS (R) Base, and good knowledge of SAS (R) graph and SAS (R) Macros. + Capable ... + Excellent application development skills. + Strong understanding of clinical trial data and extremely hands on in data...process + Advanced knowledge of R programming + Base SAS , SAS /STAT, SAS Graph and… more
    IQVIA (11/05/25)
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  • Associate Director, Statistical Programming

    Sumitomo Pharma (Harrisburg, PA)
    …SAS , SAS Macros, SAS /STAT, SAS /Graph, SAS /SQL and SAS /ODS. + Interact with Statisticians and other clinical teams, perform ad hoc analysis and ... on LinkedIn. **Job Duties and Responsibilities** + Lead on clinical studies and manage/provide training to team members when...+ undefined + Create CDISC SDTM and ADaM files, SAS export files, Define.xml and Reviewer's + undefined +… more
    Sumitomo Pharma (10/08/25)
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