• Senior Medical Manager, Medical Affairs - Cellular…

    Gilead Sciences, Inc. (Santa Monica, CA)
    …Lead the development of scientific content for promotional and educational materials, clinical trial protocols, and regulatory submissions. + Establish and ... teams to provide medical input into ongoing and future clinical trials. + Interpret clinical trial...programs to improve understanding of cellular therapies and their clinical applications. + Monitor scientific literature and… more
    Gilead Sciences, Inc. (04/12/25)
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  • Research Administrator

    University of Southern California (Los Angeles, CA)
    …projects, including contracts, grants, clinical trials, and philanthropic funding. + Clinical Trial Administration: Manage financial aspects of clinical ... coordination in a fast-paced academic environment + 5+ years of experience in clinical trial financial management + Experience with USC systems, including… more
    University of Southern California (03/28/25)
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  • Director; Global Value, Access & Pricing;…

    BeOne Medicines (San Mateo, CA)
    …Medical Affairs, and Health Economics & Outcomes Research (HEOR) teams to shape clinical trial design and evidence-generation strategies that align with target ... this position will focus on identifying market access-related evidentiary gaps in clinical development plans that could result in a breadth of reimbursement… more
    BeOne Medicines (05/07/25)
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  • Scientific Liaison, Senior Manager, Spark Aligners

    Envista Holdings Corporation (Brea, CA)
    …ensure compliance with orthodontics regulations. - Support the preparation of clinical trial protocols, regulatory filings, and post-market surveillance ... inquiries. - Provide scientific input to new Aligners development, clinical trials, and health economics. - Monitor ...into actionable insights for diverse audiences. - Experience in clinical trial design, evidence generation, or health… more
    Envista Holdings Corporation (05/01/25)
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  • Patient Account Representative

    Robert Half Accountemps (Lompoc, CA)
    …appeals to resolve claim discrepancies and ensure proper reimbursement. * Collaborate with clinical trial teams to oversee patient accounts related to study ... Epic Software. * Utilize Dynamic Data Exchange (DDE) to monitor and update patient account information accurately. * Handle...claim discrepancies. * Background in managing patient accounts within clinical trial operations is a plus. *… more
    Robert Half Accountemps (05/24/25)
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  • AVP, Complex Claim Liability Specialist-Business…

    Travelers Insurance Company (Sacramento, CA)
    …and resolve the company's most severe and/or complex Life Science medical products, clinical trial and pharmaceutical bodily injury claims, as well as General ... + CLAIM HANDLING: + Directly handle assigned severe/complex Life Science medical products, clinical trial and pharmaceutical bodily injury claims, as well as… more
    Travelers Insurance Company (05/03/25)
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  • Senior Medical Director

    Astrix Technology (San Diego, CA)
    …the development and review of regulatory filings, including INDs, CTAs, and clinical trial documentation related to RNA-targeting therapies. **Education & ... **Senior Medical Director** Clinical Data Management San Diego, CA, US Pay...and study frameworks. + Serve as medical lead and monitor for early-phase studies, including first-in-human trials, ensuring thorough… more
    Astrix Technology (05/16/25)
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  • Director, Safety Scientist

    BeOne Medicines (Emeryville, CA)
    …Lead signal assessment documentation following BeiGene signal management and safety governance framework. Clinical Trial Support + Lead the review of safety data ... and monitor the safety of patients on allocated clinical trials. + Lead the writing and review safety sections and provide safety expertise for development of… more
    BeOne Medicines (04/02/25)
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  • Senior Regulatory Affairs Specialist - Vascular…

    Abbott (Santa Clara, CA)
    …+ Previous experience with PMA / IDE and international submissions + Experience with IDE trial strategy and post market clinical activities + Ability to work in ... compliance. **Premarket:** + Assess the acceptability of quality, preclinical and clinical documentation for submission filing. + Compile, prepare, review and submit… more
    Abbott (04/29/25)
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  • Senior Director Global Regulatory Lead (Early…

    Lilly (San Francisco, CA)
    …as needed to inform development and manage issues. For preclinical and early clinical development programs, the GRL leads the US and Canada submissions and agency ... documents by leveraging team expertise, as well as scientific, drug/device clinical development and knowledge from health authorities such as regulatory policies,… more
    Lilly (05/28/25)
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