• Clinical Research Coordinator II/CPT…

    Cedars-Sinai (Los Angeles, CA)
    …The database is also used to monitor subject participation, assure regulatory compliance , and manage inventory. Collectively, MIRIAD's capabilities permit ... are maintained in association with the triad of accurate longitudinal clinical metadata, comprehensive genotype information, and serotypes. These resources are made… more
    Cedars-Sinai (09/10/25)
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  • Manager, Clinical Nutrition - Sharp Chula…

    Sharp HealthCare (Chula Vista, CA)
    …certification, and other mandatory training within established timeframes.Assists in achieving compliance with regulatory agency standards, including state and ... are made by our recruitment and hiring teams. **What You Will Do** The Clinical Nutrition Manager plans, coordinates, and manages the work operations of the … more
    Sharp HealthCare (09/13/25)
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  • Clinical Research Coordinator - Immune…

    Dana-Farber Cancer Institute (Boston, MA)
    …ensuring the timely collection and shipment of protocol-required samples, maintaining regulatory binders, and ensuring compliance with all institutional, state, ... auditing and study monitoring visits. + Coordination and management of clinical trials, including communication with Sponsors and regulatory authorities.… more
    Dana-Farber Cancer Institute (07/23/25)
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  • Clinical Research Manager

    Stanford University (Stanford, CA)
    …Manage clinical research operations, including quality management, personnel management, regulatory compliance , and fiscal oversight. **We are looking for an ... Clinical Research Manager **School of Medicine, Stanford, California,...reports to Institutional Review Board, CSTA, FDA and other regulatory agencies. Submit Investigational New Drug applications to the… more
    Stanford University (09/13/25)
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  • Clinical Documentation Improvement…

    ZoomCare (Tigard, OR)
    …reviewing outpatient clinical documentation to ensure accuracy, completeness, and compliance with coding and regulatory requirements. This role focuses on ... compliance and workflow efficiency. + Stay current on industry standards, regulatory updates, and coding guidelines that impact clinical documentation and… more
    ZoomCare (09/11/25)
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  • Lead Clinical Therapy (LIMHP) Crisis…

    Omaha Children's Hospital (Omaha, NE)
    …patient care by holding staff accountable to established patient care and regulatory standards. Interprets policies and procedure to clinical and ... difference where it matters most. **A Brief Overview** Performs a variety of clinical lead functions including leading and coordinating the daily clinical more
    Omaha Children's Hospital (09/09/25)
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  • Cancer Clinical Research Coordinator 2…

    Stanford University (Stanford, CA)
    …study specific milestones, and invoice sponsors according to study contract. + Ensure regulatory compliance . Regularly inspect study document to ensure ongoing ... Cancer Clinical Research Coordinator 2 - Radiation Oncology (Hybrid)...regulatory compliance . + Work with principal investigator to ensure Investigational… more
    Stanford University (09/09/25)
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  • Cancer Clinical Research Coordinator 2…

    Stanford University (Stanford, CA)
    …study specific milestones, and invoice sponsors according to study contract. + Ensure regulatory compliance . Regularly inspect study document to ensure ongoing ... Cancer Clinical Research Coordinator 2 - Breast Oncology (Hybrid)...regulatory compliance . + Work with principal investigator to ensure Investigational… more
    Stanford University (09/09/25)
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  • Clinical Research Coordinator II | School…

    Emory Healthcare/Emory University (Atlanta, GA)
    …Review Board applications and renewals. Also, experience maintaining Investigator Site Files/ Regulatory Binders is helpful. + Ensures compliance with research ... to the excellence of our academic community. **Description** The Clinical Research Coordinator II handles administrative activities generally associated with… more
    Emory Healthcare/Emory University (09/07/25)
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  • Senior Clinical Scientist - Ophthalmology

    Merck (North Wales, PA)
    …Analysis, Ethical Standards, ICH GCP Guidelines, Medical Writing, Motivation Management, Regulatory Compliance , Regulatory Documents, Science, Scientific ... This includes the ability to: + Solid knowledge of clinical research regulatory requirements (eg, GCP and...Adaptability, Clinical Data, Clinical Operations, Clinical Study Design, Clinical Trial Compliance more
    Merck (09/05/25)
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