• 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 (08/26/25)
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  • Principal Analyst, Clinical Programming…

    AbbVie (North Chicago, IL)
    …Biostatistics, Computer Science, Mathematics or related Scientific area, & 6 years of SAS Programming experience in clinical trials. Of the experience require, ... Science, Mathematics or related Scientific area, & 3 years of SAS Programming experience in clinical trials. Of experience required, must have 3 years of (i),… more
    AbbVie (08/21/25)
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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 (07/26/25)
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  • Senior Scientist, Statistical Programming

    Merck (Rahway, NJ)
    …Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 3 years SAS programming experience in a clinical trial environment OR a ... 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 environment. **Minimum requirement:** + Must have experience… more
    Merck (07/23/25)
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  • Senior Scientist, Biostatistics - Oncology

    J&J Family of Companies (San Diego, CA)
    …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 (08/30/25)
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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 (08/16/25)
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  • IT Solution Analyst III Medical Device Integration

    Banner Health (CA)
    …required. Strong technical skills as appropriate for position (SQL/Ansi SQL, SAS , Tableau, Excel, clinical software applications, etc.). PREFERRED QUALIFICATIONS ... making a positive change in people's lives - apply today. The Integrated Clinical Technology team is responsible for the design, build, implementation, and support… more
    Banner Health (08/20/25)
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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 (08/22/25)
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  • Senior Statistical Programmer FSP

    Cytel (Boise, ID)
    …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 (07/24/25)
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  • Senior Statistical Programmer FSP

    Cytel (Cambridge, 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...to support or lead one or more Phase I-IV clinical trials. This role can be performed as fully… more
    Cytel (08/02/25)
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