• Clinical Data Management Programmer

    United Therapeutics (Research Triangle Park, NC)
    …and pulmonary diseases, and other orphan diseases. **How you'll contribute** The Clinical Data Management Programmer is responsible for both programming and ... for phase I - IV clinical & non- clinical trials. The CDM Programmer will create...Support DM team with design, validation, and implementation of clinical databases for designated studies + Assist… more
    United Therapeutics (01/02/25)
    - Save Job - Related Jobs - Block Source
  • Programmer Analyst III - SPH - Coordinating…

    UT Health (Houston, TX)
    Programmer Analyst III - SPH - Coordinating Center for Clinical Trials **Location:** Texas Medical Center-Houston, Texas **Hot** **Category:** Information ... where you come in. **We are seeking a Full-Time Programmer Analyst III to join the Coordinating Center for... Analyst III to join the Coordinating Center for Clinical Trials within the Biostatistics & Data Science department… more
    UT Health (12/05/24)
    - Save Job - Related Jobs - Block Source
  • Senior Data Programmer Analyst

    Dana-Farber Cancer Institute (Boston, MA)
    The Senior Data Programmer Analyst under the Associate Director, Data Analysis and Management, will be key to the completion of outcomes and translational research ... studies and within the breast oncology center (BOC) and...works closely with investigators, directors, program and project managers, clinical research coordinators, research data specialists, computational biologists and… more
    Dana-Farber Cancer Institute (11/01/24)
    - Save Job - Related Jobs - Block Source
  • EDC Programmer

    ThermoFisher Scientific (Cambridge, MA)
    …development and delivery of life-changing therapies. As part of our clinical research portfolio, our CorEvitas evidence-based solutions specialize in generating data ... intelligence and clinical insights needed to bring safe and effective treatments...Data Management (CDM) team, the EDC (Electronic Data Capture) Programmer is responsible for the design, programming, compliance, and… more
    ThermoFisher Scientific (01/24/25)
    - Save Job - Related Jobs - Block Source
  • Associate Statistical Project Leader,…

    Sanofi Group (Cambridge, MA)
    …relevant statistical matters: + 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 (01/08/25)
    - Save Job - Related Jobs - Block Source