• Clinical Research Coordinator 1

    University of Miami (Miami, FL)
    regulatory bodies. Knows the contents and maintenance of study-specific clinical research regulatory binders. Maintains requisite skills and mandatory ... side effects of treatment to the Investigator and ensures Regulatory is provided accurate information to report to IRB....and registration of patients entered onto Cancer Center sponsored clinical trials are performed in compliance with… more
    University of Miami (08/01/25)
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  • Diagnostic XRay Supervisor

    Penn Medicine (Plainsboro, NJ)
    …+ Continuously improve unit/department operations to maintain and exceed internal/external regulatory compliance and achieve clinical excellence. + ... communicate to the staff, and develop/implement action plans to improve performance. + Regulatory Compliance : (In partnership with Leadership Team) + Ensures … more
    Penn Medicine (09/03/25)
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  • Clinical Documentation Specialist

    Community Health Systems (Naples, FL)
    …support continuity of care, appropriate quality metrics, and regulatory compliance . **Essential Functions** + Analyzes inpatient clinical records to identify ... Experience in physician education or query processes preferred + Familiarity with regulatory standards and quality metrics related to clinical documentation… more
    Community Health Systems (09/13/25)
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  • Supervisor Clinical Nursing / Emergency

    Omaha Children's Hospital (Omaha, NE)
    …and people with disabilities. **A Brief Overview** Performs a variety of clinical supervisory functions including leading and coordinating the daily clinical ... care by holding staff accountable to established patient care and regulatory standards. Interprets policies and procedure to nursing staff and patients/families.… more
    Omaha Children's Hospital (09/10/25)
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  • Senior Clinical Director, Oncology Early…

    Merck (Upper Gwynedd, PA)
    …Research, Mentorship, Plan of Action and Milestones (POA&M), Regulatory Affairs Compliance , Regulatory Compliance {+ 5 more} **Preferred Skills:** **Job ... clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. **Responsibilities:** Specifically, the Senior Director… more
    Merck (09/09/25)
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  • Senior Principal Scientist, Clinical

    Merck (Rahway, NJ)
    …Research, Pulmonary Disease Treatment, Pulmonary Disorders, Pulmonology, Regulatory Affairs Compliance , Regulatory Compliance , Scientific Consulting {+ 1 ... + Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development… more
    Merck (09/06/25)
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  • Clinical Research Technician

    University of Michigan (Ann Arbor, MI)
    …authorities, working closely with study monitors, and resolving issues that invariably arise. REGULATORY COMPLIANCE : The CRT is expected to ensure that all ... essential regulatory documents; reporting of adverse events; understanding of good clinical practice (GCP); and ensuring compliance with federal, state, and… more
    University of Michigan (08/22/25)
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  • Clinical Research Manager-Psychiatry…

    Mount Sinai Health System (New York, NY)
    Clinical Trials Manager will work to ensure the operational success and regulatory compliance of a growing portfolio of research studies focused on mental ... to a multidisciplinary team of coordinators and research staff, ensuring compliance with institutional policies, ethical standards, and regulatory requirements.… more
    Mount Sinai Health System (08/13/25)
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  • Clinical Research Leader - JJMT…

    J&J Family of Companies (Irvine, CA)
    …the Clinical R&D Department to execute and manage company sponsored clinical trials, ensuring compliance with timelines and study milestones. + ... etc), contributing to cross-functional alignment. + May provide on-site procedural protocol compliance and data collection support to the clinical trial sites.… more
    J&J Family of Companies (09/11/25)
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  • Clinical Research Associate I - Miriad IBD…

    Cedars-Sinai (Los Angeles, CA)
    …protocol and research objectives. Responsible for completing case report forms, entering clinical research data, and assist with regulatory submissions to the ... clinical research data from source documents. + Ensures compliance with protocol and overall clinical research...for long term follow-up patients only. + Assists with regulatory submissions to the Institutional Review Board (IRB) including… more
    Cedars-Sinai (08/27/25)
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