• Pharmacometrics Senior Manager

    Gilead Sciences, Inc. (Foster City, CA)
    …program** **Evaluate and apply state-of-the-art quantitative pharmacology approaches for clinical pharmacology decision-making and for global regulatory ... will include all stages of drug development from first-in human through Phase IV clinical trials. You will be responsible for the conduct as well as interpretation… more
    Gilead Sciences, Inc. (10/13/25)
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  • Perfusionist II

    Stanford Health Care (Palo Alto, CA)
    …collection, data base maintenance and analysis of all Perfusion data related to research , cost analysis, and clinical outcome studies. + Manages and monitors ... role goes far beyond the technical. They are trusted clinical partners to surgeons and anesthesiologists, called on to...to equipment use and maintenance; and may participate in research programs. ▪ Able to perform duties as shift… more
    Stanford Health Care (10/28/25)
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  • Global Operations Asset Leader (Goal)

    Genentech (South San Francisco, CA)
    **The Position** **The Position:** At Roche/Genentech Pharma Product Development Global Clinical Operations (PDG), we are determined to transform drug development ... our assets. This people leadership position holds significant accountability for clinical operations strategy and execution as well as enterprise collaboration.… more
    Genentech (10/14/25)
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  • Assistant Director, GMP Quality Systems

    Kelly Services (Carlsbad, CA)
    …you're connected to a wealth of future opportunities in the field of science and clinical research . \#P1 As part of our promise to talent, Kelly supports those ... Kelly(R) Science & Clinical is seeking an Assistant Director, GMP Quality...work will directly support our commitment to patient safety, regulatory excellence, and continuous improvement. **Responsibilities** + Lead and… more
    Kelly Services (09/30/25)
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  • Precision Medicine - Medical Affairs Director…

    Merck (Sacramento, CA)
    …other related disciplines + Formal training in health economics and/or outcomes research \#eligibleforERP **Required Skills:** Benefit Programs, Clinical Data, ... accurate information across the full oncology product portfolio, precision medicine, clinical science, and quality management in a balanced and credible manner… more
    Merck (10/25/25)
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  • Director of Product Marketing

    Edwards Lifesciences (Irvine, CA)
    …knowledge of current literature, current competitive environment, and regulatory /legal requirements for multiple major/high value products launches, programs, ... * Drive marketing collateral/labeling through all relevant legal and regulatory approval processes through collaboration with relevant cross-functional stakeholders… more
    Edwards Lifesciences (09/18/25)
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  • Scientist III, Bioinformatics (Cap/Clia/CDx)

    ThermoFisher Scientific (West Sacramento, CA)
    …maintain bioinformatics pipelines, analyze complex genomic data, ensure compliance with regulatory standards, and support clinical validations and data ... **Collaboration:** Work closely with cross-functional teams, including laboratory scientists, clinical researchers, regulatory professionals, and software developers,… more
    ThermoFisher Scientific (10/23/25)
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  • Medicare Formulary Strategy Manager

    Elevance Health (Costa Mesa, CA)
    …+ Research market trends, evaluate competitive positioning, and assess the regulatory landscape to guide GRS clinical program strategies. **Governance & ... and execution within a regulated healthcare environment. + Ability to synthesize clinical , financial, and regulatory insights into actionable strategies. +… more
    Elevance Health (10/31/25)
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  • Senior Manager, Statistics

    AbbVie (South San Francisco, CA)
    …areas. + Support or lead GMA Statistics group in partnership with GMA, Clinical Research and Clinical Statistics to develop scientifically appropriate ... implementation.Provide statistical leadership for design, analysis and reporting for clinical or other scientific research programs.Independently develop… more
    AbbVie (10/24/25)
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  • Principal MDR - Vigilance Specialist

    Medtronic (Los Angeles, CA)
    …Adverse Drug Experience (ADE) data or adverse reaction data as required by regulatory agencies Review and analyze clinical databases for the extraction of ... biggest health challenges with healthcare technology. We fuse technology and research for groundbreaking solutions. From less-invasive surgery that minimizes a… more
    Medtronic (09/30/25)
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