• Research Coordinator 1 (NE S UAW Research)

    University of Washington (Seattle, WA)
    …exceeds these requirements. There are multiple resources available within the University system (eg Grant and Contract Services, Institutional Review Board, ... compliance, and to ensure accurate and reliable data collection. Assist in monitoring and administering patient protocol , interacting closely with clinical… more
    University of Washington (11/13/25)
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  • Clinical Research Associate

    Actalent (Houston, TX)
    …site management and monitoring activities comply with ICH-GCP, SOPs, Clinical Monitoring Plan, Protocol , study plans, local laws, and regulations. + Verify ... a dedicated Clinical Research Associate (CRA) responsible for managing and monitoring clinical trial activities at assigned study sites, ensuring compliance with… more
    Actalent (12/12/25)
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  • RN Clinical Research

    HCA Healthcare (Austin, TX)
    …research and study protocols . Screens and recruits patients based on protocol criteria . Explains study protocols, procedures and treatments to patients and ... with Pharmacist if on Delegation Log . Administers Investigational Drug as per protocol . Serve as a resource for department members for medical interpretations of… more
    HCA Healthcare (09/21/25)
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  • Senior Clinical Trial Physician, Rheumatology

    Bristol Myers Squibb (Madison, NJ)
    …support of cross-portfolio activities in line with Clinical Excellence, including Protocol Review Committee, support of Business Development activities and ... of across portfolio activities in line with Clinical Excellence, including eg Protocol Review Committee, support of Business Development activities and Quality… more
    Bristol Myers Squibb (12/03/25)
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  • Senior Clinical Trial Manager, FSP

    ThermoFisher Scientific (Wilmington, NC)
    …level:** Global CTM experience, highly experienced in CRO and monitoring oversight, with strong vendor management skills **Summarized Purpose:** Accountable ... data from evaluable patients as specified in the study protocol ) within the time period specified in the contract...Reg, CMC etc ): ensure feasibility report are exhaustive, Review site feasibility reports as per oversight plan ,… more
    ThermoFisher Scientific (10/25/25)
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  • Senior Clinical Sciences Professional

    University of Colorado (Aurora, CO)
    …subject's medical history, CGM, insulin pump, and current medication information, review the research protocol inclusion/exclusion criteria, and confirm the ... and train junior team members. + Develops or assists with developing protocol -specific systems and documents, including process flows, training manuals, Standard… more
    University of Colorado (12/14/25)
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  • Clinical Site Lead - Los Angeles

    Abbott (Pleasanton, CA)
    …identify and obtain missing data, data corrections, reviewing adverse events and protocol deviations. + Review data and source documentation from investigational ... Management, EP, Structural Heart, and Heart Failure). Recognized resource in protocol execution, increasing product and disease state knowledge, procedure support… more
    Abbott (11/01/25)
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  • Clinical Research Coordinator (Oncology) - #Staff

    Johns Hopkins University (Baltimore, MD)
    …assisting database design, approval, and implementation, amendment management, subject eligibility review , and monitoring regulatory and subject compliance for ... information. + Obtain and maintain excellent operating knowledge of assigned clinical protocol , clinical equipment, and clinical computer systems . + Oversee… more
    Johns Hopkins University (11/26/25)
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  • Quality Improvement Manager

    Sevita (Las Vegas, NV)
    …for incidents involving alleged abuse and/or neglect + Implement the Incident Management Protocol and Mortality Review Protocol in addition to Operating ... Management + Oversee the implementation of the incident reporting system according to our Incident Management Protocol ...+ Compliance + Develop and oversee quality and compliance monitoring systems to measure the state's compliance… more
    Sevita (12/09/25)
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  • Sr Clinical Research Data Specialist

    University of Rochester (Rochester, NY)
    …and is responsible for the compilation, registration and submission of data, monitoring compliance with the protocol , adherence to Standard Operating Procedures ... limited to, requirements gathering, writing test plans, data collection system build, peer code review and quality...program design and testing; package selection and use of systems , software and equipment. Offers solutions and suggestions to… more
    University of Rochester (11/15/25)
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