• Clinical Research Nurse I

    ICON Clinical Research (San Antonio, TX)
    …experience, preferably in a research or academic healthcare setting, with exposure to clinical trial operations and Good Clinical Practice (GCP) guidelines. ... Clinical Research Nurse I- Full Time Permanent (M-F...participant recruitment, and retention throughout the duration of the trial . + Providing education and counseling to study participants… more
    ICON Clinical Research (11/20/25)
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  • Senior Manager, Clinical Partner…

    Takeda Pharmaceuticals (Boston, MA)
    …procurement, contract management, or supplier relationship management + Strong knowledge of clinical trial processes and regulatory requirements + Experience in ... commercial constructs + Sound understanding of GCP, ICH guidelines, and clinical trial regulations + Strong strategic thinking and project management skills +… more
    Takeda Pharmaceuticals (11/20/25)
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  • Director, PMO - Clinical

    Stryker (Fremont, CA)
    …core laboratories, CROs, consultants, etc. as appropriate to ensure safe and successful clinical trial conduct. + Meets with KOLs, study Principal Investigators ... to orchestrate the success of the portfolio. This position will be in the Clinical discipline focused on, 1. Shaping and Implementing the global clinical more
    Stryker (11/20/25)
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  • Clinical Research RN Coordinator - Cardiac…

    University of Southern California (Arcadia, CA)
    …and conducts quality assurance reviews. This position also addresses/resolves clinical trial patient complaints and schedules/coordinates/performs testing and/or ... Trials. + Compliance with Informed Consent Process. + Management of Clinical Trial Patients. + Ensure that Documentation meets all regulatory and compliance… more
    University of Southern California (11/19/25)
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  • Part-time Research Services Clinical

    University of Colorado (Aurora, CO)
    …protocol inclusion/exclusion criteria, and confirms eligibility of subject to participate in clinical trial . + Perform informed consent process or ensures that ... phone contacts and personal interviews. + Schedule subject participation in research clinical trial , coordinating availability of necessary space, and … more
    University of Colorado (11/19/25)
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  • Open Rank Research Services Clinical

    University of Colorado (Aurora, CO)
    …protocol inclusion/exclusion criteria, and confirms eligibility of subject to participate in clinical trial . + Perform informed consent process or ensures that ... phone contacts and personal interviews. + Schedule subject participation in research clinical trial , coordinating availability of necessary space, and … more
    University of Colorado (11/19/25)
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  • Senior Clinical Supply Associate

    ICON Clinical Research (PA)
    …You Will Be Doing:** + Managing the planning, coordination, and execution of clinical trial supplies to ensure timely and compliant distribution. + Collaborating ... clinical supply chain management, with a deep understanding of clinical trial processes and regulatory standards. + Strong organizational and project… more
    ICON Clinical Research (11/19/25)
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  • Senior Director, Clinical Trials- Winship…

    Emory Healthcare/Emory University (Atlanta, GA)
    …supported to meet these expectations and requirements with a concentrated focus on increasing clinical trial accrual to meet the needs of the Winship catchment ... with faculty, staff, and other cancer-related organizations to raise awareness of clinical trial offerings. Organize and run meetings with stakeholders (disease… more
    Emory Healthcare/Emory University (11/17/25)
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  • Clinical Research Medical Director,…

    Amgen (Washington, DC)
    …interactions. + Provide clinical /scientific input during the development and execution of clinical trials + Interpret clinical trial data + Participate ... commercialization processes + Experience with developing study concepts for clinical development and clinical trial ...developing study concepts for clinical development and clinical trial designs with cross functional input,… more
    Amgen (11/14/25)
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  • Clinical Research Associate I - Urology

    Cedars-Sinai (Los Angeles, CA)
    …Safety Letters in accordance with local and federal guidelines. *Assists with clinical trial budgets. *Assists with patient research billing. *Schedules patients ... that is at the forefront of medical advancements! The Clinical Research Associate I (CRAI) will work directly with...Academic / Research **Job Specialty** : Research Studies/ Clin Trial **Overtime Status** : NONEXEMPT **Primary Shift** : Day… more
    Cedars-Sinai (11/13/25)
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