• Principal Statistical Programmer

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

    Cytel (Boston, MA)
    …be a part of this new program. **Position Overview:** As a Senior Statistical Programmer , you will leverage your advanced SAS programming skills and proficiency ... heart of our client's innovation. As a Senior Statistical Programmer you will be dedicated to one of our...Science, Mathematics, etc. + At least 8 years of SAS programming working with clinical trial data… more
    Cytel (04/25/25)
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  • Principal Statistical Programmer

    Parexel (Newton, MA)
    …3) ICH-GCP, CDISC, and WSOP guidelines; 4) Analyzing data from Phase I, II, and III clinical trials; 5) SAS /BASE, SAS /STAT, SAS /SQL, SAS /MACRO, ... of Employer:** Parexel International LLC **Position Title:** Principal Statistical Programmer **Position Location:** 275 Grove Street, Newton, MA 02466 **Hours:**… more
    Parexel (07/02/25)
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  • Principal Statistical Programmer FSP - RWD

    Cytel (Cambridge, MA)
    …background rates) for the development of regulatory/safety documents, and Clinical Development (eg; assessment of patient populations/ protocol feasibility). + ... level proficiency in SQL is a must. In addition, SAS or R proficiency is required. + Deep expertise...Market Clarity), , Truveta and UK Biobank. Experience analyzing clinical trial and/or registry data is desirable. + Familiarity… more
    Cytel (06/17/25)
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  • Associate Statistical Project Leader

    Sanofi Group (Cambridge, MA)
    …**Main Responsibilities:** + Provide high quality input into the design of the clinical study (including protocol development), the setup and conduct of the study to ... as the quality control plan. + Perform and/or coordinate with study programmer the production of statistical analyses. Review and examine statistical data… more
    Sanofi Group (07/03/25)
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