• Senior Manager, Program Resource Management (PRM)

    Amgen (Thousand Oaks, CA)
    …will be accountable for forecasting, allocating and overseeing resourcing for our global clinical trial delivery team. Using your ability to analyze, interpret ... research vendors (CRO's, central labs, imaging vendors, etc.) + Knowledge of clinical trial processes & operations is preferred **What you can expect of us** As… more
    Amgen (08/24/25)
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  • Vice President, Strategic Sourcing

    Vera Therapeutics (Brisbane, CA)
    …including establishment of best practices for vendor selection and qualification for clinical trial services, RFP development and management, bid analysis and ... across all supply chain activities, including vendor compliance. * Oversee clinical trial readiness, including compliant labeling, packaging, and documentation… more
    Vera Therapeutics (08/09/25)
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  • Territory Manager, Structural Heart, TAVI…

    Abbott (Sacramento, CA)
    …use of Navitor with FlexNav and other portfolio devices used in commercial and clinical trial cases. + Evaluates patient anatomy and valve sizing for customers ... that the assigned territory meets or exceeds sales and clinical objectives of the Structural Heart TAVI division. This...division. This role is responsible for commercial accounts and trial sites in assigned territory reporting into the Regional… more
    Abbott (07/18/25)
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  • Senior Biostatistician

    J&J Family of Companies (Irvine, CA)
    …at professional meetings. + Stay current with statistical methodology in clinical trial design and analysis. **Functional and Technical Competencies:** ... will be responsible for designing statistical analysis plans for clinical studies; performing statistical analyses independently; creating reports intended for… more
    J&J Family of Companies (08/20/25)
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  • Associate Medical Director, Pharmacovigilance…

    Sumitomo Pharma (Sacramento, CA)
    …marketed products. + Conduct safety surveillance over product life cycle, reviewing clinical trial and post-marketing Individual Case Safety Reports (ICSRs), ... to medical safety of clinical trials, including monitoring of clinical trial safety and laboratory data. + Generates safety queries, evaluates safety data… more
    Sumitomo Pharma (08/15/25)
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  • Associate Director, Pipeline Analytics

    BeOne Medicines (San Carlos, CA)
    …predictive models and scenario analysis frameworks to assess asset progression probability, clinical trial outcomes, and market access feasibility. + Utilize ... optimizing patient segmentation and treatment pathways. + Strong understanding of clinical trial design, regulatory pathways, and market access considerations.… more
    BeOne Medicines (08/15/25)
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  • Counsel, Intellectual Property

    Sumitomo Pharma (Sacramento, CA)
    …and negotiating for various types of agreements, including licensing agreements, clinical trial agreements, sponsored research agreements, material transfer ... + JD with 5+ years of patent litigation experience, with patent pre- trial and trial experience in US District Courts. + Preferred experience in managing… more
    Sumitomo Pharma (09/03/25)
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  • RayzeBio Associate Director - Biostatistical…

    Bristol Myers Squibb (San Diego, CA)
    …outputs based on protocols/SAP + Participate in reviewing, analyzing, and reporting clinical trial data and generating outputs to support DSUR/IBs, publications, ... + Advanced Knowledge with FDA and ICH regulations and guidelines, and clinical trial methodologies. + Good written and verbal communication skills. + Be able… more
    Bristol Myers Squibb (08/30/25)
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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 (08/08/25)
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  • Senior Statistical Programmer FSP

    Cytel (Sacramento, CA)
    …spanning all therapeutic areas. + Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS ... Mathematics, etc. + At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor's degree or… more
    Cytel (07/24/25)
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