• Medical Director, Oncology Early Development

    Genentech (South San Francisco, CA)
    …therapies to benefit patients. **The Opportunity:** This role focuses on the clinical trial development of innovative anti-cancer therapies across Genentech's ... + Ideally 0-2 years of industry experience in oncology or comparable clinical trial experience in an academic setting + Excellent scientific record with… more
    Genentech (09/06/25)
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  • Sr. CRA, Sponsor Aligned, Oncology

    IQVIA (Carlsbad, CA)
    … Research Associate! You'll play a pivotal role in monitoring and managing clinical trial sites to ensure compliance with study protocols, regulations, and ... phases as required. Documentation: Ensure all site documents are filed in the Trial Master File (TMF) and Investigator's Site File (ISF) per GCP/ICH and local… more
    IQVIA (11/06/25)
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  • Principal Biostatistician

    Parexel (Sacramento, CA)
    …work remotely. The Principal Biostatistician works independently on all level complexity clinical trial projects, often with major regulatory impact. The person ... Accountabilities** : **Operational Execution** + Provide broad statistical support, including trial design, protocol and CRF development on specific studies + Lead… more
    Parexel (11/22/25)
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  • Corporate Paralegal (Contract)

    Allogene (South San Francisco, CA)
    …master service agreements and associated work orders, material transfer agreements, and clinical trial agreements). * Manage the contract lifecycle, including ... material transfer agreements and associated work orders, supply chain agreements, and clinical trial agreements. * Strong understanding of corporate governance… more
    Allogene (11/12/25)
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  • Regulatory Coordinator II - Heart Institute…

    Cedars-Sinai (Los Angeles, CA)
    …research files and documentation involving the regulatory requirements for the study/ clinical trial . Other duties include, representing the Research Department ... the Medical Center during these meetings. + Works closely with the clinical trial coordinator, research staff, and investigators to assure that all regulatory… more
    Cedars-Sinai (10/01/25)
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  • Financial Systems Specialist

    Aston Carter (South San Francisco, CA)
    …apply AI tools and other emerging technologies to accounting workflows. + Support clinical trial expense accruals, working closely with Clinical Operations ... Familiarity with automation tools and continuous improvement methodologies. + Exposure to clinical trial accruals or biotech/life sciences accounting. + Strong… more
    Aston Carter (11/25/25)
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  • Contracts Administrator

    Aston Carter (South San Francisco, CA)
    …consulting agreements, supply and vendor contracts, master service agreements, and clinical trial agreements. + Manage the contract lifecycle, including ... agreements, master service agreements, material transfer agreements, supply chain agreements, and clinical trial agreements. Work Environment This is a hybrid… more
    Aston Carter (11/22/25)
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  • Medical & Technical Writer, Sci Ops - JJMT…

    J&J Family of Companies (Irvine, CA)
    …**Preferred Skills:** Clinical Evaluation Reports, Clinical Operations, Clinical Research and Regulations, Clinical Trial Designs, Literature ... at https://www.jnj.com **Job Function:** R&D Operations **Job Sub** **Function:** Clinical /Medical Operations **Job Category:** Professional **All Job Posting Locations:**… more
    J&J Family of Companies (11/27/25)
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  • Study Coordinator

    UCLA Health (Los Angeles, CA)
    clinical trials research budgeting process to assist with the preparation of clinical trial budgets. + Working knowledge of FDA Code of Federal Regulations ... Department of Medicine is seeking a skilled and motivated Clinical Research Coordinator to support the full lifecycle of... Research Coordinator to support the full lifecycle of clinical research studies, from initial design and study start-up… more
    UCLA Health (11/26/25)
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  • MCS Supply Chain Sr. Associate

    US Tech Solutions (Thousand Oaks, CA)
    clinical supplies (ie GxP, GDP guidelines, GMP guidelines, ICH guidelines, Clinical Trial Directive) + Strong communication, verbal & written, presentation ... dose and is involved throughout the durations of the clinical studies and programs until study closure. The study...direction, the GSP manages the following responsibilities for assigned clinical studies. + Manage forecast demand and supply for… more
    US Tech Solutions (11/26/25)
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