• Clinical Affairs Manager, in vitro diagnostics

    ThermoFisher Scientific (South San Francisco, CA)
    …the Design History File (DHF) project. + Interact as the primary clinical studies representative to Pharmaceutical partners concerning IVD study requirements. + ... primary role of this position is targeted toward Clinical Studies planning, core team support, and CRO Management. In...the primary responsibilities include: + Participate as a clinical study representative for project core teams. + Participate in… more
    ThermoFisher Scientific (12/10/25)
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  • US Medical Senior Director, Medical Affairs…

    Gilead Sciences, Inc. (Santa Monica, CA)
    …(eg, retrospective, prospective, interventional, RWE) to address the unmet needs. ** Study Oversight and Execution** + Provide scientific and medical oversight for ... all Medical Affairs / Kite Sponsored Studies including interventional trials, non-interventional studies , and...US Strategic Alliances. + Lead the development of clinical study concepts, protocols in collaboration with Medical and Clinical… more
    Gilead Sciences, Inc. (12/11/25)
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  • Executive Director, Global Clinical Supply Chain…

    Gilead Sciences, Inc. (Foster City, CA)
    …clinical supply for the overall development portfolio, including clinical development programs and studies at all phases as well as managed access programs. May lead ... and robust resource allocation for PDM sub-teams and clinical study teams. + Partners across several PDM functions and...(OTIF) delivery of IMP to initiate and resupply clinical studies . + Responsible for decision-making and direct the long-term… more
    Gilead Sciences, Inc. (11/12/25)
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  • Assistant Clinical Research Coordinator (Hybrid…

    Stanford University (Stanford, CA)
    …related to the collection of clinical data and/or the coordination of clinical studies for lung transplant patients. This position will work under the general ... which offer potentially promising therapeutic benefits, as well as outcome studies which characterize clinical parameters to effect positive changes in patient… more
    Stanford University (12/05/25)
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  • Clinical Research Coordinator III - Cardiology…

    Cedars-Sinai (Los Angeles, CA)
    …research?** The Clinical Research Coordinator III works independently providing study coordination including screening of potential patients for protocol ... details, and participating in the informed consent process. Responsible for oversight of all studies with the group and the assignment of studies to clinical… more
    Cedars-Sinai (11/02/25)
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  • Night Sleep Technologist

    Sleep Data (San Diego, CA)
    …The Sleep Technologist is responsible for preparing and conducting sleep studies in accordance with established protocols, including verifying medical orders, ... patient experience, with every patient interaction. + Prepare for sleep studies by reviewing patient history, verifying medical orders, and following established… more
    Sleep Data (11/21/25)
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  • Senior Director, Clinical Operations Lead, Biotech…

    BeOne Medicines (San Mateo, CA)
    …Unit at regional and global level and ensure timely, quality, and efficient study planning and execution of associated clinical programs/ studies + Conduct ... accountable for the planning, budget, and oversight the execution of clinical studies of BTU assets, through partnering with execution units, that ensures clinical… more
    BeOne Medicines (11/08/25)
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  • Biostatistics Oncology Lead, Early Development

    Genentech (South San Francisco, CA)
    …Management to enable data-driven decision-making from first-in-human through proof-of-concept studies . As trusted partners in early development, we design efficient ... the statistical strategy across multiple programs, define best practices for study design and evidence generation, and drive methodological excellence in exploratory… more
    Genentech (10/11/25)
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  • Associate Director, Clinical Science

    Bristol Myers Squibb (San Diego, CA)
    …on functional area activities during program implementation, clinical study start-up/execution/close out, data analysis/reporting, and potentially support of ... trial design to develop or oversee development of specific study concept synopses and protocols. + Participates in protocol...with team members to ensure scientific integrity of clinical studies . + May be sought out for advice by… more
    Bristol Myers Squibb (12/23/25)
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  • Clinical Research Coordinator II, Hybrid

    Cedars-Sinai (Beverly Hills, CA)
    …Description** The Clinical Research Coordinator II works independently providing study coordination including screening of potential patients for protocol ... response to sponsor queries. Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and… more
    Cedars-Sinai (12/13/25)
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