• Associate Director, Biostatistics

    BeOne Medicines (San Mateo, CA)
    …and interprets results from clinical trials to meet objectives of the study protocol . Applies and implements basic and complex techniques to these analyses under ... supervision. + Prepares oral and written reports to effectively communicate results of clinical trials to the project team. + Provides responses to queries relating to study design, analysis, and interpretation posed by the clinical monitors, regulatory… more
    BeOne Medicines (09/23/25)
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  • Senior Clinical Research Associate

    BeOne Medicines (Emeryville, CA)
    …products and/or medical devices * Conduct site visits to determine protocol and regulatory compliance, and prepare required documentation * Develop collaborative ... relationships with investigative sites, and study vendors * Track enrollment status reports to ensure study sites stay on track to meet enrollment goals * Track study-specific status reports to ensure all required information regarding site issues, deviations,… more
    BeOne Medicines (09/17/25)
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  • Research Coordinator I

    University of Southern California (Los Angeles, CA)
    …other hospital personnel. The Coordinator is accountable to the Medical Director and Associate Director of CISO and to the Principal Investigators with whom he/she ... not restricted to those listed below. Specific Job Functions I. Research A. Protocol Related 1. On request from supervisor, reviews in-house protocols prior to CIC… more
    University of Southern California (11/19/25)
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  • Clinical Research Coordinator I, Laboratory…

    Cedars-Sinai (Los Angeles, CA)
    …a moderate degree of proficiency and understanding of research protocol and laboratory procedures, including centrifuging, aliquoting, storing, and shipping ... documents. + Facilitates screening and recruitment of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients,… more
    Cedars-Sinai (09/06/25)
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  • Clinical Site Lead - Los Angeles

    Abbott (Pleasanton, CA)
    …appropriate collaboration with Abbott clinical staff, eg Site CRA, Site Contract Associate . + Train facility staff regarding protocol requirements and ... 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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  • Windows Administrator

    GovCIO (Sacramento, CA)
    …Certification (ie, Microsoft Certified Solutions Expert(MCSE), Server+, Cisco Certified Network Associate (CCNA), RedHat, Palo, etc.,can be waived for 30 days after ... senior level fundamental knowledge in networking principles, + Transmission Control Protocol /Internet Protocol (TCP/IP), Domain Name System (DNS), Dynamic Host… more
    GovCIO (09/24/25)
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  • Research Nurse Coordinator II (Hybrid),…

    Cedars-Sinai (Beverly Hills, CA)
    …a wide range of research activities - from conducting detailed protocol assessments and performing intradermal injections, to educating patients, providing nursing ... care to research participants. Utilizes clinical nursing background and extensive research protocol knowledge to serve as a liaison between nursing staff, Principal… more
    Cedars-Sinai (11/15/25)
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  • Nuclear Med/PET/CT Technologist - Sharp Chula…

    Sharp HealthCare (Chula Vista, CA)
    …identifiers.* Verification of order (electronically or written prescription).* Accurately associate the patient to their images and ordered procedure.Review the ... area(s) and appropriate person(s).Consistently participates and document the Universal Protocol (patient verification, side/site marking and time-out) as appropriate.Assists… more
    Sharp HealthCare (11/09/25)
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  • Clinical Research Coordinator II - The Angeles…

    Cedars-Sinai (Los Angeles, CA)
    …II to join our team. The ideal candidate will have a minimum of an Associate Degree or College Diploma and at least 3 years of clinical research coordination or ... planning, projecting resource requirements, and developing systems to ensure protocol compliance and patient safety. + Coordinates administrative functions of… more
    Cedars-Sinai (09/04/25)
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  • Sr. CRA, Sponsor Aligned, Oncology

    IQVIA (Carlsbad, CA)
    Job Overview: Join our dynamic team as a Clinical Research Associate ! You'll play a pivotal role in monitoring and managing clinical trial sites to ensure compliance ... plans, ensuring project needs are met. Training & Communication: Provide protocol and study training to sites, maintaining regular communication to manage… more
    IQVIA (11/06/25)
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