• Clinical Research Coordinator III, BMT / Clinical…

    Children's Hospital Los Angeles (Los Angeles, CA)
    …and familiarity with transplant-related adverse event reporting. * Proficiency in managing regulatory documentation for BMT trials, including IND submissions and ... and stem cell therapies, which require specialized coordination and regulatory oversight. Responsibilities include managing investigational product logistics, monitoring… more
    Children's Hospital Los Angeles (09/03/25)
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  • Director, Data Content Acquisition

    S&P Global (CA)
    …SPDJI's custom and branded indices. Ensure adherence to licensing, reporting and regulatory requirements. . Manage global data rights, review agreements for legal ... scorecards, and other internal risk mitigation processes . Assist with any regulatory compliance exercises and vendor audits **Functional & Business Knowledge:** .… more
    S&P Global (08/30/25)
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  • Medical Billing Specialist III/IV - Behavioral…

    Ventura County (Ventura, CA)
    …Medi-Cal Provider Manual and TAR process, they ensure timely, compliant submissions that support access to behavioral health services. They communicate effectively ... Medi-Cal, Medicare, and Commercial Insurance, they ensure accuracy, efficiency, and regulatory adherence in all mental health billing operations. Medical Billing… more
    Ventura County (08/27/25)
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  • Managed Care Coordinator

    Cedars-Sinai (Los Angeles, CA)
    …Agreement (LOAs), while also managing credentialing tasks, onboarding, and regulatory reporting. The position also supports departmental budgeting processes, ... (RFIs) from health plans and payers for specialty services, reviewing submissions for appropriateness and advancing concerns (eg, financial or contract-related data)… more
    Cedars-Sinai (08/21/25)
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  • Research Nurse Coordinator I, Oncology (Hybrid)

    Cedars-Sinai (Beverly Hills, CA)
    …clinical study coordination, subject Screening/recruitment/enrollment, data management/integrity, regulatory compliance, project/study evaluation and interfaces with ... department process (grade, attribution, treatment, etc), and reports to regulatory and sponsor as required. + Records research data...and ensures protocol is followed. + May prepare IRB submissions . + May process, ship, track or otherwise handle… more
    Cedars-Sinai (08/21/25)
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  • Sr Labeling Lead

    Terumo Neuro (Aliso Viejo, CA)
    …and international standards along with cross-functional input from Marketing, R&D, Regulatory Affairs, and Legal. Job duties: + Responsible for end-to-end labeling ... to develop labels that meet the needs of customers and all regional regulatory requirements. + Plan and execute label development schedule, ensuring timely delivery… more
    Terumo Neuro (08/10/25)
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  • Director, Accounting - Assistant Controller

    L3Harris (Sacramento, CA)
    …Accepted Accounting Principles (GAAP) and full compliance with all relevant regulatory requirements, including the International Traffic in Arms Regulations (ITAR) ... overseeing all accounting activities, ensuring compliance with accounting standards, regulatory requirements, and internal financial policies. The Director of… more
    L3Harris (08/03/25)
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  • Risk Manager, Extended Producer Responsibility,…

    Amazon (San Diego, CA)
    …optimize compliance processes, and support Amazon's goals while navigating complex regulatory landscapes. Key job responsibilities - Lead the end-to-end process of ... registration and reporting obligations with public authorities, ensuring timely submissions and maintaining accurate documentation while developing automated tracking… more
    Amazon (07/30/25)
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  • Senior Scientist I, Biologics Drug Substance…

    AbbVie (South San Francisco, CA)
    …highly experienced scientists and managers who have directly enabled the development/IND submissions of 20+ novel oncology drugs and successfully filed two BLAs. The ... and review technical reports, GMP campaign summary reports and relevant sections in regulatory filings + Actively seek out opportunities to optimize our platform or… more
    AbbVie (07/18/25)
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  • Director, Human Factors Engineering…

    Gilead Sciences, Inc. (Foster City, CA)
    …for device design history files and HFE sections for health authority submissions and written responses. + Educate team members and other internal stakeholders ... all HFE work is performed in accordance with SOPs and applicable regulatory requirements. **Required Education, Experience & Skills:** + A Bachelor's degree in… more
    Gilead Sciences, Inc. (06/24/25)
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