• Clinical Study Build…

    Lilly (Indianapolis, IN)
    …for people who are determined to make life better for people around the world. The ** Clinical Study Build Programmer - eCOA** is responsible for ... technology, data flow, data standards, database programming, normalization and testing. The Clinical Study Build Programmer will collaborate with Data… more
    Lilly (07/30/25)
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  • Clinical Study Build…

    Lilly (Indianapolis, IN)
    …for people who are determined to make life better for people around the world. The Clinical Study Build Programmer is responsible for programming and ... the mapping, testing and normalization of data into a clinical data warehouse. This requires an in-depth understanding of...MHRA, FDA, ICH, GCP, PhRMA, Privacy knowledge, etc.) to study build deliverables + Integrates multi-functional and/or… more
    Lilly (07/30/25)
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  • Senior Clinical Data Science…

    ICON Clinical Research (MN)
    …development + Metadata rave certified REQUIRED + BS Degree + Medidata Rave EDC Certified Study Builder + This is a hybrid position. Candidates must work 3 days ... must either have : * **Medidata Rave EDC Certified Study Builder ** or at least the equivalent...least the equivalent combination of both * **Medidata Rave Study Design and Build Essentials (SDBE)** **Pay… more
    ICON Clinical Research (08/28/25)
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  • Principal Programmer Analyst

    ThermoFisher Scientific (West Greenwich, RI)
    …lead and innovate within a best-in-class team, driving technological advancements in clinical trials. Summarized Purpose: As a Principal Programmer Analyst, you ... and advising less expert team members. Leads's programming, project oversight, and study strategy coordination for clinical trials. Coordinates team efforts,… more
    ThermoFisher Scientific (09/05/25)
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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 ... the quality control plan. + Perform and/or coordinate with study programmer the production of statistical analyses....into interpretation and discussion of results sections for the clinical study report (CSR) and/or publications to… more
    Sanofi Group (09/09/25)
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