• Associate Medical Director/Medical Director…

    ThermoFisher Scientific (Greenville, NC)
    …and supports business development activities. Provides medical review and analysis for clinical trial serious adverse events, marketed products ICSR and periodic ... modules, etc. to ensure that the medical content is accurate and complete. ** Clinical Trial Support:** + Monitors all safety variables (AE, laboratory… more
    ThermoFisher Scientific (10/09/25)
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  • Associate Director, Biostatistics

    Otsuka America Pharmaceutical Inc. (Raleigh, NC)
    …As core study/project team member, provide statistical input in different perspective of the clinical trial conduct such as CRF review, IRT setting, DMC set up, ... products for the maintenance of everyday health. As an Associate Director, Biostatistician, you will be a champion of... clinical , statistical, and regulatory literature for current clinical trial results, regulatory trends and new… more
    Otsuka America Pharmaceutical Inc. (11/20/25)
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  • Senior Precision Medicine Associate - FSP

    Parexel (Raleigh, NC)
    … clinical trials. Performs other duties as necessary to ensure optimal clinical trial execution. **Key Accountabilities** **:** **Study Team Support** + ... has an exciting opportunity for a Senior Precision Medicine Associate . This role works closely with line Manager, Precision...collection procedures and presentation slides) + Manages acquisition of clinical trial samples + Provides support for… more
    Parexel (11/08/25)
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  • Associate Director, Regulatory Affairs…

    ThermoFisher Scientific (Greenville, NC)
    …and non-promotional materials to ensure global compliance. + Manages global Clinical Trial Authorization (CTA) submissions and strategy, aligning labeling ... Supply Chain to ensure accurate and timely implementation of labeling decisions. + ** Clinical Trial Regulatory Responsibilities** + Develop and oversee global … more
    ThermoFisher Scientific (11/23/25)
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  • Associate / Medical Director - Rheumatology…

    Parexel (Raleigh, NC)
    …in Lupus is preferred *Experienced as a Physician in Industry or as a clinical trial investigator with significant clinical research experience The ability ... experience treating rheumatology patients clinically and/or who possess extensive rheumatology clinical trial related experience will be considered for this… more
    Parexel (10/11/25)
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  • Study Start Up Associate II - Oncology…

    ICON Clinical Research (NC)
    …(Competent Authorities) to obtain all necessary authorizations/approvals pertaining to the clinical trial conduct (start up and maintenance as assigned). ... us on our mission to shape the future of clinical development. **Study Start Up Associate II**...as identified. + Ensure accuracy and timely completeness of Trial Master File (TMF) documents submitted during start-up and… more
    ICON Clinical Research (11/21/25)
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  • Patient Recruitment Associate I

    ICON Clinical Research (Rocky Mount, NC)
    …clinical research network, where you'll play a key role in transforming the clinical trial experience for patients and sponsors alike. Our global site network ... Patient Recruitment Associate - Rocky Mount, NC (Hybrid) ICON plc...questions + Review, enter, and edit patient information into clinical trial management software + Book patients… more
    ICON Clinical Research (11/14/25)
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  • Health Technician (Telehealth Clinical…

    Veterans Affairs, Veterans Health Administration (Greenville, NC)
    Summary The Health Technician (Telehealth Clinical ) - Advanced provides high level support, training, and advanced management of telehealth operations and is ... typically stationed at a clinical care delivery site (VA Medical Center, CBOC, VA...will be required to serve a 1 or 2-year trial period during which we will evaluate your fitness… more
    Veterans Affairs, Veterans Health Administration (11/25/25)
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  • Associate Director, Regulatory Affairs…

    Sumitomo Pharma (Raleigh, NC)
    …regulatory submissions and working with regulatory templates + Understanding of EU Clinical Trial Regulation and ROW country regulatory requirements related to ... a dynamic, highly motivated, and experienced individual for the position of ** Associate Director, Regulatory Affairs (Oncology).** The Associate Director is part… more
    Sumitomo Pharma (10/11/25)
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  • CRA 2, Early Clinical Development, IQVIA…

    IQVIA (Durham, NC)
    …candidates located East, Central or West Coast. **Job Overview** We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key ... IQVIA Early Clinical Development is hiring for CRA 2. Ideal...essential documents are collected and maintained in both the Trial Master File (TMF) and the Investigator Site File… more
    IQVIA (11/01/25)
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