• Global Clinical Study

    BeOne Medicines (Emeryville, CA)
    …of clinical study processes + Able to independently lead large and/or complex global clinical studies + 5 or more years of progressive experience in ... timelines and budget + Leads all aspects of assigned clinical study (ies) + Leads global ...over the study life cycle + Ensures clinical studies at a project level are… more
    BeOne Medicines (12/30/25)
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  • Regional Clinical Study Senior…

    BeOne Medicines (Emeryville, CA)
    …provides regular updates on study progress in the region to senior management and Global Clinical Study Manager as required + Represents the regional ... and budget + Acts as regional lead for multiple studies across an indication or across a program as...Clinical Study Report in collaboration with Global Clinical Study Manager more
    BeOne Medicines (12/20/25)
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  • Regional Clinical Study

    BeOne Medicines (Emeryville, CA)
    …provides regular updates on study progress in the region to senior management and Global Clinical Study Manager as required + Represents the regional ... Clinical Study Report in collaboration with Global Clinical Study Manager...and the quality of the work performed on assigned studies + Contributes to development, optimization and review of… more
    BeOne Medicines (10/29/25)
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  • Executive Director, GCO Franchise Head

    BeOne Medicines (Emeryville, CA)
    …Head will lead and manage the Global Clinical Program Lead (GCPL)/ Global Clinical Study Manager (gCSM) group in designated Franchise(s)- ... efficient study planning and execution of associated clinical programs/ studies + Conduct regular program review...and lead efforts to deepen scientific knowledge within the Clinical Operations' function + Champions a global more
    BeOne Medicines (11/07/25)
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  • Associate Director, Regional Clinical

    BeOne Medicines (Emeryville, CA)
    …_Line management responsibilities:_ + Provides leadership, management, and/or mentorship to clinical study managers at various levels for assigned portfolio ... external stakeholders within the region as well as with global stakeholders to ensure the needs of the business...of the business are met. + Contributes to overall Clinical Operations strategy for the region and is accountable… more
    BeOne Medicines (11/11/25)
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  • Senior Clinical Trial Manager

    GRAIL (Menlo Park, CA)
    …on-site activities. **Responsibilities:** + Serves as the Clinical Operations Study Lead for assigned studies , providing strategic and operational leadership ... are using the power of next-generation sequencing (NGS), population-scale clinical studies , and state-of-the-art computer science and...For more information, please visit grail.com . The Sr. Clinical Trial Manager serves as a … more
    GRAIL (10/03/25)
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  • Senior Manager , Clinical Science,…

    Edwards Lifesciences (San Francisco, CA)
    …is responsible for providing scientific expertise throughout the development and implementation of clinical studies and clinical evaluations for a dynamic ... clinical science and medical writing deliverables. + Lead clinical study design and clinical ...and accurate data reporting. + Summarize key data from clinical studies and published literature and provide… more
    Edwards Lifesciences (10/17/25)
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  • Senior Clinical Data Manager

    GRAIL (Menlo Park, CA)
    …and we are using the power of next-generation sequencing (NGS), population-scale clinical studies , and state-of-the-art computer science and data science to ... For more information, please visit grail.com . The Senior Clinical Data Manager (CDM) will lead data...management activities for one or multiple diagnostic product development studies in support of GRAIL's robust clinical more
    GRAIL (12/04/25)
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  • Lead Clinical Data Manager (Remote)

    IQVIA (San Francisco, CA)
    …with all necessary equipment provided._ **What You'll Do** + Lead data management for complex, global clinical trials from study setup to database lock. + ... Management Leads to oversee end-to-end data management delivery for global clinical trials. You'll ensure quality, accuracy,...Management Project Manager_ . + Proven success managing large global studies (1000+ patients). + Expertise with… more
    IQVIA (10/31/25)
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  • Sr. Manager , Clinical Research…

    Taiho Oncology (Pleasanton, CA)
    …to support the creation of relevant high-quality clinical documents such as study protocols and clinical study reports (CSRs), investigator brochures, ... conferences and leverages the knowledge for designing and summarizing clinical studies . + Keeps Sr. Medical Director...as reviewing of the quality of ongoing and final clinical study data, protocols and CSRs, investigator… more
    Taiho Oncology (12/23/25)
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  • Senior Manager , Clinical Supply…

    BeOne Medicines (Emeryville, CA)
    …to planning, label development, label & pack, and distribution for one or more clinical studies . Actively develops and oversees supply plans to ensure accurate ... provides leadership and guidance during process implementations. **Essential Functions:** + Represent the Clinical Supply Chain on Clinical Study Teams (CST)… more
    BeOne Medicines (12/15/25)
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  • Oncology Late Stage Clinical Scientist…

    Pfizer (South San Francisco, CA)
    …informed consent documents, and contributes to authoring of IBs, site training materials, clinical study reports, regulatory responses, and other clinical ... for programs within the Late-Stage Oncology portfolio. **KEY RESPONSIBILITIES** + Clinical development expert for assigned studies maintaining current scientific… more
    Pfizer (11/16/25)
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  • Manager , Clinical Supply Chain

    BeOne Medicines (Emeryville, CA)
    …successful study management **Supervisory Responsibilities:** + Demonstrates knowledge of global clinical trials and the drug development process. + ... **General Description:** The Manager of Clinical Supply Chain manages...for the future. **Essential Functions** : + Represent the Clinical Supply Chain on Clinical Study more
    BeOne Medicines (12/11/25)
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  • Senior Clinical Trial Physician,…

    Bristol Myers Squibb (Brisbane, CA)
    …across the internal and external network * Manages Phase 2 to Phase 3 clinical studies , with demonstrated decision-making capabilities * This role will include ... of medical accountability and oversight for one or more clinical trials within the Global Drug Development...late clinical development needs and adequacy of clinical studies leading to registration **Qualifications &… more
    Bristol Myers Squibb (11/19/25)
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  • Senior Manager , Clinical Supply…

    BeOne Medicines (Emeryville, CA)
    …Lead and depot PM setting up distribution and return/destruction procedures for studies following the logistics related procedures. + Coordinate drug destruction at ... internal audit and external audit as needed on logistics data preparation per study or compound level. + Facilitate and coordinate with courier and depot vendors… more
    BeOne Medicines (12/18/25)
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  • Senior Manager , Global Procurement…

    BeOne Medicines (Emeryville, CA)
    …The primary focus will be on services and products to support our clinical and commercial studies & products including small molecule manufacturing, large ... **General Description:** The Senior Procurement Manager of CMO Category is responsible for establishing,...Pharmaceutical Ingredients related CMOs. This role will reside in Global Tech Ops Procurement to establish standard business processes… more
    BeOne Medicines (12/17/25)
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  • Clinical Research Associate I

    Abbott (Alameda, CA)
    clinical data listings for completeness and accuracy; and escalate issues to the Clinical Operations Manager / Study Lead as needed. + Proactively and ... monitoring and site management activities, ensuring compliance to the Study Protocol, Good Clinical Practices (GCPs), ICH...effectively communicate the status of clinical studies to management. + Participate in… more
    Abbott (11/18/25)
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  • Clinical Scientist, Early Development

    Bristol Myers Squibb (Brisbane, CA)
    Clinical Scientist function provides scientific expertise necessary to design and deliver clinical studies and programs. + Will be responsible for design and ... study team meetings in partnership with GDO protocol manager and collaborate with cross-functional study team...the protocol in collaboration with Data Management/Programming + Submit clinical contributions to clinical study more
    Bristol Myers Squibb (12/24/25)
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  • EDC/ Clinical Devices Research Coordinator

    US Tech Solutions (South San Francisco, CA)
    Clinical Trial Manager and PI, is responsible for independently conducting clinical research sessions with study participants. + These sessions will be ... Research Coordinator activities for assigned clinical research device studies including consenting participants, conducting study sessions, maintaining… more
    US Tech Solutions (10/17/25)
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  • Director, Clinical Pharmacology…

    Bristol Myers Squibb (Brisbane, CA)
    …strategy teams and on relevant governance forums + Provides input to Phase 2/3 clinical study design and registrational strategy + Supervises the development of ... Clinical Pharmacology Plan(s) + Supervises design of Clinical Pharmacology studies and manages data analysis,...talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our… more
    Bristol Myers Squibb (12/06/25)
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