• (Senior) Data Team Lead

    IQVIA (Anaheim, CA)
    …Matter Expert (SME). Comply with Good Clinical Practices (GCPs), applicable regulatory guidelines, SOPs, policies, and, where available, CDM guidance documents. ... DTL staff. + Independently maintain internal tracking databases and systems Financial Management/Business Development Support: + Independently manage SOW/budget +… more
    IQVIA (08/01/25)
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  • Bilingual Clinical Research Associate I - Ramin…

    Cedars-Sinai (Los Angeles, CA)
    …for completing case report forms, entering clinical research data, and assist with regulatory submissions to the IRB. Provides limited patient contact as needed for ... (CRFs). + Enters clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors. +...for long term follow-up patients only. + Assists with regulatory submissions to the Institutional Review Board (IRB) including… more
    Cedars-Sinai (08/01/25)
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  • Associate Director Sales Channel/Affiliates…

    Wolters Kluwer (Sacramento, CA)
    …to help save lives, improve the way we do business, build better judicial and regulatory systems . We help them get it right. **Who We Are: Wolters Kluwer: ... on comprehensive data analysis. + Ensure department compliance with company and regulatory standards. + Drive innovation in sales and marketing programs to improve… more
    Wolters Kluwer (08/01/25)
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  • Director of Global Logistics

    Sonos (Santa Barbara, CA)
    …transportation, customs, and trade compliance to ensure seamless product flow and regulatory adherence. + Direct the global reverse logistics and RMA operations to ... + Strong expertise in international trade compliance, customs, and regional regulatory requirements. + Proven ability to drive cost optimization, implement logistics… more
    Sonos (08/01/25)
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  • Associate Manufacturing

    Amgen (Thousand Oaks, CA)
    …that include periods of rigorous, repetitive work + Working around high-pressure systems and occasionally working around heavy equipment + Available to work various ... as appropriate to the individual area + Ability to adhere to regulatory requirements, written procedures and safety guidelines + Ability to evaluate… more
    Amgen (07/31/25)
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  • Senior Manager, GCP Auditor

    BeOne Medicines (Emeryville, CA)
    …GCP regulations and industry standards, in accordance with applicable regulatory requirements, guidelines, laws and internally established standards and practices. ... resources with relevant stakeholders: Review documentation, procedures, and quality management systems prior to conducting audits. + Conducting Audit : Perform… more
    BeOne Medicines (07/30/25)
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  • Director Facilities & Co-Generation

    Trinity Health (Fresno, CA)
    …Health's mission, values, and operational standards while driving performance, regulatory compliance, and cost-effective service delivery. The Director provides ... interpreting construction documents (plans and specifications). 7. Knowledge of relevant regulatory standards and agencies including EPA, NFPA, OSHA, TJC, and DNV.… more
    Trinity Health (07/25/25)
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  • Senior Counsel- Product Development & Marketing

    Western Digital (Sacramento, CA)
    …to some of the largest and highest-growth organizations in the world. From enabling systems to make cities safer and more connected, to powering the data centers ... product launch and distribution, customer support, warranty, and related product regulatory concerns + Maintain current understanding of best practices related to… more
    Western Digital (07/25/25)
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  • Director, Drug Metabolism

    Gilead Sciences, Inc. (Foster City, CA)
    …CROs to assure high quality and timely delivery of written PK reports and regulatory documents (IND, IMPD, IB, BLA) for regulatory submissions. + Supervising of ... and application of mechanistic PK-PD and multi-compartmental modeling using software systems such as Phoenix/WinNonlin, MATLAB/Simbiology, or similar. + Knowledge in… more
    Gilead Sciences, Inc. (07/24/25)
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  • Senior Clinical Research Associate

    BeOne Medicines (Emeryville, CA)
    …medical devices * Conduct site visits to determine protocol and regulatory compliance, and prepare required documentation * Develop collaborative relationships with ... PowerPoint and Outlook * Familiar with industry CTMS and data management systems **Other Qualifications:** * Understands clinical trial processes with a thorough… more
    BeOne Medicines (07/23/25)
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