• Senior Statistical Programmer FSP

    Cytel (Boston, MA)
    …you'll be at the heart of our client's innovation. As a Senior Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company ... this new program. **Position Overview:** As a Senior Statistical Programmer , you will leverage your advanced SAS programming skills...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 (with R)

    Cytel (Boston, MA)
    …you'll be at the heart of our client's innovation. As a Senior Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company ... this new program. **Position Overview:** As a Senior Statistical Programmer , you will leverage your advanced SAS programming skills...to support or lead one or more Phase I-IV clinical trials. This role can be performed as fully… more
    Cytel (07/19/25)
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  • Mainframe Programmer

    Eliassen Group (Boston, MA)
    **Mainframe Programmer ** **Anywhere** **Type:** Contract **Category:** Development **Industry:** Financial Services **Workplace Type:** Remote **Reference ID:** JN ... their technology solutions, financial, risk & compliance, and advisory solutions, and clinical solutions. With offices from coast to coast and throughout Europe,… more
    Eliassen Group (07/30/25)
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  • Senior Principal Database Developer

    Cytel (Boston, MA)
    Experienced Medidata RAVE programmer to maintain Rave URL and be the point of contact for other teams using Medidata applications such as CTMS, eCOA, Safety Gateway. ... other Medidata applications + At least 12 years progressive Clinical Research Experience + Medidata Rave Certified Study Builder...Study Builder + 10 years' experience as a database programmer + Zelta certified builder a plus, but not… more
    Cytel (07/23/25)
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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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