• Sr. Clinical Research Associate - FSP

    Parexel (Sacramento, CA)
    …investigators. + In some countries, as required, CRAs are accountable for study start - up and regulatory maintenance. Tasks may include Site Qualification ... the application process; submission of proper application/documents to EC/IRB and to Regulatory Authorities for start - up and for the duration of the study. +… more
    Parexel (12/10/25)
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  • Master Instrumentation/Calibration Technician…

    Genentech (South San Francisco, CA)
    …diagnostics, calibration, and maintenance of industrial process systems and instruments, ensuring regulatory compliance. + Support systems start - up and ... Support:** + Provide technical and leadership oversight during the design, installation, start - up , and commissioning of process equipment and critical utilities.… more
    Genentech (11/22/25)
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  • Coordinator - START

    YAI (Fresno, CA)
    …active caseload of up to 20 - 25 individuals referred for START Services and provides systemic consultation based on assessment and outreach findings, using ... combination of education, experience and/or training as authorized by START /NCSS and/or appropriate State regulatory agency...authorized by START /NCSS and/or appropriate State regulatory agency (eg OPWDD, etc.); however, all START more
    YAI (11/19/25)
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  • Clinical Research Coordinator Associate

    Stanford University (Stanford, CA)
    …include:** + Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start - up through close-out. ... of an assigned set of research protocols assuring efficiency and regulatory compliance. Other responsibilities will include recruiting, screening, assisting in the… more
    Stanford University (12/08/25)
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  • Clinical Research Coordinator Associate

    Stanford University (Stanford, CA)
    …include:** + Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start - up through close-out. ... forms for completion and accuracy with source documents. Prepare regulatory submissions and ensure Institutional Review Board renewals are...hand, lift, carry, push, and pull objects that weigh up to 40 pounds. + Rarely kneel, crawl, climb… more
    Stanford University (12/08/25)
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  • Clinical Research Associate I

    Abbott (Alameda, CA)
    …procedures, and other applicable regulatory requirements. + Participate in study start up activities. + Assist with shipping study devices and supplies ... and final reviews of study data in preparation of regulatory submissions. + May interact with RA/QA in responding...management. + Working knowledge of CFR, ICH-GCP, Clinical and Regulatory Affairs + Proficient with Microsoft Suite **What We… more
    Abbott (11/18/25)
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  • Order Selector - 4AM Start - EPJ Experience…

    Lineage Logistics (Fontana, CA)
    Use pallet jack equipment to assemble customer orders while following all regulatory and company safety standards, policies, and procedures. Deliver product to the ... in temperatures as low as -20 Fahrenheit/-25 Celsius in cold storage sites or up to 100 Fahrenheit/37 Celsius in dry storage sites while wearing company provided… more
    Lineage Logistics (01/03/26)
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  • Order Selector - 3PM Start

    Lineage Logistics (Fullerton, CA)
    …tall, and prepare products for shipment- while following all company and regulatory safety standards. **KEY DUTIES AND RESPONSIBILITIES** + Operate **electric pallet ... to work in temperatures as low as **-20 F / -25 C** in cold storage or up to **100 F / 37 C** in dry storage while wearing company-provided PPE and freezer gear… more
    Lineage Logistics (12/31/25)
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  • Clinical Research Coordinator Associate

    Avispa Technology (Palo Alto, CA)
    …Responsibilities: * Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start - up through ... case report forms for completion and accuracy with source documents. Prepare regulatory submissions, and ensure Institutional Review Board renewals are completed. *… more
    Avispa Technology (01/08/26)
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  • Regional Clinical Study Senior Manager

    BeOne Medicines (Emeryville, CA)
    …submissions of study in countries in assigned region in close collaboration with regional study start up team and regulatory affairs + Ensures regional and ... timelines + Generates, manages, and maintains high quality study start up and recruitment timelines for region...local drug labels for region. Provides input on local regulatory approval and reimbursement status of comparator drugs used… more
    BeOne Medicines (12/20/25)
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