• Associate , Clinical Trial

    Sumitomo Pharma (Raleigh, NC)
    …are currently seeking a dynamic, highly motivated, and experienced individual for the position of ** Clinical Trial Associate (CTA)** **.** The Clinical ... conduct of clinical trials and handling administrative aspects of clinical trial execution. This role will support completion of all study deliverables,… more
    Sumitomo Pharma (09/10/25)
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  • Associate , Start-up Clinical…

    Sumitomo Pharma (Raleigh, NC)
    …currently seeking a dynamic, highly motivated, and experienced individual for the position of ** Clinical Trial Associate for Study Start-up** **.** The ... Clinical Trial Associate for Study Start-up (SSU CTA) assists in the delivery of site start up activities for assigned studies from site identification… more
    Sumitomo Pharma (09/10/25)
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  • Clinical Research Associate 2

    Grifols Shared Services North America, Inc (Research Triangle Park, NC)
    …set-up, central lab set-up, and other vendor selection processes.** + **Maintaining clinical trial management system (CTMS) information pertaining to the study ... **Knowledge, Skills, and Abilities:** Good knowledge of medical terminology, protocol, clinical trial process, regulatory requirements, and company SOPs. Good… more
    Grifols Shared Services North America, Inc (08/08/25)
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  • Associate Director Clinical…

    GRAIL (Durham, NC)
    …and provide compliance advice on SOPs, processes, and protocols for both clinical trial and companion diagnostic activities, ensuring consistency and compliance ... with pharmaceutical companies for companion diagnostic (CDx) tests. The Associate Director, Clinical Compliance will play a...of applicable regulations and standards as they relate to clinical trial conduct + Understanding of appropriate… more
    GRAIL (08/02/25)
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  • Clinical Research Associate…

    IQVIA (Durham, NC)
    …applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... IQVIA is hiring a Clinical Research Associate with on-site monitoring...required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's… more
    IQVIA (07/04/25)
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  • (Senior) Clinical Research Associate…

    IQVIA (Durham, NC)
    …applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. *… more
    IQVIA (07/14/25)
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  • Associate Medical Director/Med Dir…

    ThermoFisher Scientific (Wilmington, 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 (08/08/25)
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  • CRA 2/Sr. CRA 1, Early Clinical…

    IQVIA (Durham, NC)
    …to join our team. In this role, you will be responsible for monitoring clinical trial sites to ensure compliance with study protocols, regulatory guidelines, and ... IQVIA Biotech is hiring for our Early Clinical Development team. Ideal candidates will have Phase...site documentation is properly maintained and filed in the Trial Master File (TMF) and Investigator Site File (ISF)… more
    IQVIA (09/10/25)
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  • Regulatory Associate

    University of North Carolina- Chapel Hill (Chapel Hill, NC)
    …regulatory and compliance actions through completion on study team trackers and in clinical trial management system * Providing updates (oral and/or written) on ... binder, including entering regulatory and study information in the electronic clinical trial management system (OnCore) and eRegulatory binder (Florence).… more
    University of North Carolina- Chapel Hill (08/28/25)
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  • Associate Medical Director,…

    Sumitomo Pharma (Raleigh, NC)
    …marketed products. + Conduct safety surveillance over product life cycle, reviewing clinical trial and post-marketing Individual Case Safety Reports (ICSRs), ... highly motivated, and experienced individual for the position of ** Associate Medical Director.** The Associate Medical Director...safety of clinical trials, including monitoring of clinical trial safety and laboratory data. +… more
    Sumitomo Pharma (08/15/25)
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