• Sr. Scientist, Statistical Programming- PKPD…

    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 (06/24/25)
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  • Senior Statistical Programmer, Late Stage…

    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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  • 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 (05/28/25)
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  • Senior Scientist, Statistical Programming

    Merck (North Wales, PA)
    …Applied Mathematics, Life Sciences, Engineering or related field plus at least 3 years SAS programming experience in a clinical trial environment. + **OR** a ... Engineering or related field plus at least 5 years SAS programming experience in a clinical trial...5 years SAS programming experience in a clinical trial environment. **Positions Required skills and expereince:** +… more
    Merck (04/25/25)
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  • Associate Principal Scientist, Statistical…

    Merck (North Wales, PA)
    …Applied Mathematics, Life Sciences, Engineering or related field plus at least 7 years SAS programming experience in a clinical trial environment OR a Bachelor's ... Life Sciences, Engineering or related field plus 9 years SAS programming experience in a clinical trial...9 years SAS programming experience in a clinical trial environment. **Required Skills and Experience:** + Experience… more
    Merck (05/10/25)
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  • Senior Scientist, Biostatistics

    J&J Family of Companies (Raritan, NJ)
    …the organization, building working relationships with therapeutic area leaders, internal SAS programmers, clinical trial managers, and personnel from regulatory ... in the tumor microenvironment. **Key Responsibilities:** + Provide statistical input into the clinical development of drugs for treatment of cancer. + Work with the … more
    J&J Family of Companies (06/14/25)
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  • Senior SAS Research Programmer - USC…

    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/Senior- ... and private and public sector engagement, is looking for aSenior SAS Research Programmerto provide programming support on research projects examining health… more
    University of Southern California (05/17/25)
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  • Senior Statistical Programmer (Remote)

    WCG Clinical (Cary, NC)
    …**JOB SUMMARY:** A Senior Statistical Programmer plays a pivotal role in analyzing clinical trial data by developing and validating SAS programs that meet ... skills, and/or ability required. + Create, test, and validate SAS programs for analyzing clinical trial data,...test, and validate SAS programs for analyzing clinical trial data, focusing on generating SDM's ADaM, tables,… more
    WCG Clinical (06/25/25)
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  • Pharmacometrics Analyst ( SAS Programming)

    AbbVie (North Chicago, IL)
    …primary responsibilities for this role include the analysis and reporting of clinical trial data without supervision for routine activities and with supervision for ... the statistical programming activities for routine studies. + Develop SAS programs for the creation of ADaM data sets...of ADaM data sets following CDISC standards. + Develop SAS programs for the creation of Tables, Listings and… more
    AbbVie (05/23/25)
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  • Senior Statistical Programmer FSP

    Cytel (Boston, MA)
    …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...or lead one or more Early or Late stage clinical trials. **This role is Hybrid office based in… more
    Cytel (04/25/25)
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