• Global Clinical Trial

    Merck (Raleigh, NC)
    …position involves a 24-36 month committed experience rotating throughout Research and Development Division/ Global Clinical Trial Operations in various ... in preparation for movement into next roles. This role will collaborate throughout Global Clinical Trial Operations local, country, and HQ levels, with… more
    Merck (11/11/25)
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  • Therapeutic Strategy Director - Respiratory

    IQVIA (Durham, NC)
    …We are looking for a Therapeutic Strategy Lead who is experienced in Respiratory global clinical trial development and can support customer engagement and ... this role, it is important to understand Respiratory disease clinical trial operations from Phase...experience with Clinical Operations and Clinical Project Management. IQVIA is a leading global more
    IQVIA (10/09/25)
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  • GYN Oncology, Regional Medical Scientific Director…

    Merck (Raleigh, NC)
    …to ensure they have a medical contact within the company. + Upon request from Global Clinical Trial Operations (GCTO), support Company-Sponsored Trials ... a specific compound or trial . + Recommend potential study sites to Global Clinical Trial Operations (GCTO)/ Clinical Research. + Address requests… more
    Merck (11/07/25)
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  • Regional Medical Scientific Director (Medical…

    Merck (Raleigh, NC)
    …to patient enrollment and retention efforts to achieve study milestones Upon request from Global Clinical Trial Operations (GCTO) + Recommends study ... policies + Maintains current knowledge and comprehension of dynamic scientific and clinical environment in the Company's Areas of Interest (AOI) **Research** Upon… more
    Merck (11/12/25)
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  • Patient Site Engagement Operations

    IQVIA (Durham, NC)
    Trial Delivery Leaders (TDLs), Trial Delivery Managers (TDMs). Interface with key Global Clinical Operations (GCO) customers Local Trial Manager ... discipline. + Minimum of 3 years relevant experience in global patient recruitment and clinical trial...preferred + Expertise in the areas of drug development, clinical trial operations , and strategic… more
    IQVIA (10/24/25)
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  • Clinical Trial Leader

    IQVIA (Durham, NC)
    **J** **ob Overview** Clinical Trial Project Leaders are an integral part of clinical trial delivery, working alongside clinical teams to improve ... by bringing new drugs to the market faster. The Clinical Trial Leader is a member of...in bid defense preparations and meetings. Develop and present Clinical Operation plan in partnership with Business… more
    IQVIA (11/13/25)
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  • Trial Master File (TMF) Specialist Oncology

    Sumitomo Pharma (Raleigh, NC)
    …Technology to ensure system validation is maintained. + Work closely with Clinical Operations and Regulatory Affairs to ensure compliance with regulatory ... Co., Ltd., is a global pharmaceutical company based in Japan with operations in the US (Sumitomo Pharma America, Inc.), focused on addressing patient needs in… more
    Sumitomo Pharma (11/05/25)
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  • Sr. Director/VP/ Clinical Delivery Lead,…

    Norstella (Raleigh, NC)
    …& analytics **Requirements** + Deep knowledge and expertise of the pharma strategic Clinical trial landscape (Clin Dev/Ops, clinical development plan ... + Protocol Design, Country, Site and Investigator Feasibility + Clinical trials operations , cost benchmarking & landscapes...+ Experience using data analytics and services to solve clinical trial challenges + Understanding of how,… more
    Norstella (11/05/25)
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  • Senior Medical Director, Clinical Research…

    Sumitomo Pharma (Raleigh, NC)
    …assigned asset(s) within the Ophthalmology therapeutic area + Provides oversight of clinical trial conduct, interacting with CROs, medical monitors, and vendors ... global pharmaceutical company based in Japan with key operations in the US (Sumitomo Pharma America, Inc.), Canada...clinical data output + Contributes to interpretation of clinical trial results and the writing of… more
    Sumitomo Pharma (09/27/25)
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  • Clinical Study Manager

    IQVIA (Durham, NC)
    …readiness quality, within agreed timelines and budget + Leads the regional clinical operations team (including oversight of external partners working on ... overall study goals **Essential Functions** + Leads the regional clinical operations team effectively, ensures effective decision...study progress in the region to senior management and Global Clinical Study Manager as required +… more
    IQVIA (11/13/25)
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  • Senior Project Manager - Global Medical…

    United Therapeutics (Research Triangle Park, NC)
    clinical studies, registries, or other strategic study/departmental initiatives. + Lead operations of clinical trial (s) from study start-up to close-out ... contracting, and management of study-related steering/advisory committees + Collaborate with clinical operations and other relevant functional groups (UT and… more
    United Therapeutics (09/26/25)
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  • Operations Technician l

    Catalent Pharma Solutions (Morrisville, NC)
    Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help ... and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments… more
    Catalent Pharma Solutions (11/03/25)
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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** + ... (lab manual, sample collection procedures and presentation slides) + Manages acquisition of clinical trial samples + Provides support for sample related matters… more
    Parexel (11/08/25)
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  • Project Manager / Senior Project Manager, Patient…

    Norstella (Raleigh, NC)
    …project roadmap development, and risk mitigation. + Deep understanding of clinical trial operations , patient recruitment strategies, regulatory ... of Citeline's Patient Engagement and Recruitment solutions, including patient-facing websites and clinical trial recruitment platforms, with a focus on complex… more
    Norstella (11/06/25)
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  • Associate Director, Regulatory Affairs (Oncology)

    Sumitomo Pharma (Raleigh, NC)
    …regulatory submissions and working with regulatory templates + Understanding of EU Clinical Trial Regulation and ROW country regulatory requirements related to ... Co., Ltd., is a global pharmaceutical company based in Japan with operations in the US (Sumitomo Pharma America, Inc.), focused on addressing patient needs in… more
    Sumitomo Pharma (10/11/25)
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  • Principal Biostatistician FSP, Late Phase

    IQVIA (Durham, NC)
    …to establish project objectives and timelines. + Write the statistical sections of clinical trial protocols, while consulting with internal and external experts. ... and availability of resources. + Collaborate with Data Management, Clinical Development, and Clinical Operations ...experience. + **At least 3 years in Phase 2/3 clinical trial experience.** + Demonstrated ability to… more
    IQVIA (09/11/25)
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  • Principal Biostatistician FSP, R Regulatory…

    IQVIA (Durham, NC)
    …to establish project objectives and timelines. + Write the statistical sections of clinical trial protocols, while consulting with internal and external experts. ... and availability of resources. + Collaborate with Data Management, Clinical Development, and Clinical Operations ...experience. + **At least 3 years in Phase 2/3 clinical trial experience.** + Demonstrated ability to… more
    IQVIA (09/08/25)
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  • Senior Specialist, Medical Writing

    Edwards Lifesciences (Raleigh, NC)
    …interventions, coronary interventions, heart failure-and current treatment landscape; familiarity with clinical research and/or clinical trial experience. + ... your ideas and expertise can change a patient's life. We generate extensive clinical evidence to demonstrate the effectiveness and safety of our innovations and how… more
    Edwards Lifesciences (09/27/25)
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  • Senior Biostatistician (FSP)

    IQVIA (Durham, NC)
    …Provide statistical input to study protocols. + Writes the statistical sections of clinical trial protocols, while consulting with internal and external experts. ... timelines, deliverables, and availability of resources. + Collaborates with Data Management, Clinical Development, and Clinical Operations on design of… more
    IQVIA (11/11/25)
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  • Principal Biostatistician FSP, Early Phase

    IQVIA (Durham, NC)
    …Provide statistical input to study protocols. + Writes the statistical sections of clinical trial protocols, while consulting with internal and external experts. ... timelines, deliverables, and availability of resources. + Collaborates with Data Management, Clinical Development, and Clinical Operations with statistical… more
    IQVIA (08/19/25)
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