• Medical Writer II

    ICON Clinical Research (New York, NY)
    …and scientific conferences. + Assisting in the review and validation of clinical data , ensuring accuracy, completeness, and consistency with study protocols, ... analytical and critical thinking skills, with the ability to review and interpret clinical data , identify key findings and trends, and communicate results… more
    ICON Clinical Research (04/17/25)
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  • ADaM Standards Engineer, FSP

    IQVIA (Durham, NC)
    …Provides technical and/or operational support in the delivery and application of industry clinical data standards within the statistical programming data ... with implementing CDISC standards that supports strategies and processes for clinical trials is required.** **Responsibilities:** + Develop, update, and maintain… more
    IQVIA (05/10/25)
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  • Associate Director, Biostatistics

    Taiho Oncology (Princeton, NJ)
    …review TFLs for the clinical trials + Analyze and help interpret clinical data + Create/author statistical sections of scientific and/or regulatory documents ... and evolving needs of patients. Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources… more
    Taiho Oncology (03/28/25)
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  • Senior Clinical Research Associate

    BeOne Medicines (San Mateo, CA)
    …a site monitor and is responsible for the management and oversight of their assigned clinical study sites to ensure data quality and patient safety in accordance ... Word, Excel, PowerPoint and Outlook * Familiar with industry CTMS and data management systems **Other Qualifications:** * Understands clinical trial processes… more
    BeOne Medicines (04/23/25)
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  • Manager CDM Study Lead

    Regeneron Pharmaceuticals (Basking Ridge, NJ)
    We are looking for a Clinical Data Manager who will serve as the DM study lead and point of contact for clinical study teams and external partners, (eg, ... to SDMs + Perform & document the oversight of CRO data management activities for assigned studies....or Masters Degree_ + _6 + years of progressive clinical data management and_ + _Study lead… more
    Regeneron Pharmaceuticals (05/09/25)
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  • Medical Director, Medical Affairs, Respiratory…

    Regeneron Pharmaceuticals (Sleepy Hollow, NY)
    …* Oversees and provides hands on support in management, generation and dissemination of clinical and non- clinical data that supports the medical strategy and ... and non-interventional respiratory clinical trials. * Attends clinical study team meetings, data oversight review...data oversight review sessions, and works closely with CRO medical monitors in support of medical affairs … more
    Regeneron Pharmaceuticals (05/14/25)
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  • Sr. Medical Writer

    Terumo Neuro (Aliso Viejo, CA)
    …producing some of the most reliable and technologically advanced products supported by proven clinical data . Take a closer look at what **Micro** Vention (R) ... Some typical job duties include: + Collaborating with the clinical & regulatory teams to write clinical ... submissions (preferably as a medical writer for pharmaceutical, CRO , or medical device clients). 4. Excellent writing and… more
    Terumo Neuro (03/04/25)
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  • Sr Med Director - Hematology/Oncology(Remote US)

    ThermoFisher Scientific (Austin, TX)
    …departments and clients. May provide oversight of medical review and analysis of data for clinical trial serious adverse events, aggregate review (eg, trending ... to drive decision-making on risk/benefit evaluation and argumentation, pharmaco-epidemiological or clinical trial data interpretation, and risk assessment, if… more
    ThermoFisher Scientific (04/13/25)
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  • Senior Manager, Programming

    Takeda Pharmaceuticals (Boston, MA)
    …participate in the weekly Study Execution Team (SET) meetings; oversee external clinical research organization ( CRO ) to ensure they meet programming ... and communicate effectively with internal cross-functional teams such as statistics, data management, clinical operations, and medical writers to ensure… more
    Takeda Pharmaceuticals (04/05/25)
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  • Principal Statistical Programmer

    IQVIA (Chicago, IL)
    …database components and theory. + Excellent application development skills. + Strong understanding of clinical trial data and extremely hands on in data ... Programmer + Home Based + Min 7+ years of CRO /Pharma Industry + Therapeutic Areas: Oncology // Immunology //...internal and external clients and (iii) the programming quality control checks for the source data and… more
    IQVIA (05/19/25)
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