• Clinical Events Committee Specialist

    Stanford University (Stanford, CA)
    …is required. + Experience in clinical trials operations, knowledge of clinical trials regulatory requirements, or experience working with an IRB. + ... Clinical Events Committee Specialist I **School...excellent communication skills in speaking and writing. + Multisite clinical trial management experience. + Some project… more
    Stanford University (05/11/24)
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  • Senior Staff Regulatory Affairs…

    Stryker (Fremont, CA)
    …research, export, and commercial distribution, such as: IDE, IDES, IDE Progress Report, Clinical Trial Submission [OUS], 510(k), PMA, PMA Annual Report, HDE, HDE ... benefits. (https://d25zu39ynyitwy.cloudfront.net/oms/000000/document/2024/6/SMVZW\_USStrykerEmployeebenefits/USStrykerEmployeebenefits.pdf) We are currently seeking a **Senior Staff Regulatory Affairs Specialist ** to join our Neurovascular… more
    Stryker (06/20/24)
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  • Senior Regulatory Affairs Specialist

    Abbott (Santa Clara, CA)
    …catheters and software, vessel closure devices and peripheral stents. This **Senior Regulatory Affairs Specialist ** position is an on-site opportunity working ... As an individual contributor, the function of a Senior Regulatory Affairs Specialist is to provide support.../ IDE and international submissions + Experience with IDE trial strategy and post market clinical activities… more
    Abbott (05/15/24)
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  • Clinical Research Operations…

    Stanford University (Stanford, CA)
    Clinical Research Operations Specialist II to conduct and manage multi-site clinical trials . Research will be conducted in a variety of therapeutic areas, ... Clinical Research Operations Specialist II **School...for promoting/recruiting research participants and retaining participants in long-term clinical trials . + Oversee data management for… more
    Stanford University (06/20/24)
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  • Senior Clinical Pharmacologist I

    Gilead Sciences, Inc. (Foster City, CA)
    …to cross-functional partners and stakeholders. + Anticipates problems that may arise in clinical trials and develops solutions for these using precedents and ... and related analysis, interpretation and reporting, and support of regulatory filings. You will typically lead clinical ...+ Able to anticipate problems that may arise in clinical trial design. + Significant knowledge of… more
    Gilead Sciences, Inc. (05/22/24)
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  • Clinical Neurotechnology Research Assistant

    Stanford University (Stanford, CA)
    …performance of clinical neurotechnology research in the homes of clinical trial participants with tetraplegia (quadriplegia). These responsibilities include ... with paralysis and their families/caregivers. These research sessions occur in the homes of clinical trial participants and may involve driving for up to three… more
    Stanford University (05/25/24)
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  • Senior Clinical Pharmacologist II

    Gilead Sciences, Inc. (Foster City, CA)
    …with regulatory agencies. + Anticipates problems that may arise in clinical trials and develops solutions for these using precedents and original ... out, PK-PD and related analysis, interpretation and reporting, and support of regulatory filings. You will typically lead clinical pharmacology cross-functional… more
    Gilead Sciences, Inc. (06/05/24)
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  • Inventory Specialist

    Sutter Health (Livermore, CA)
    …that meets the short- and long-term goals of Supply Chain and clinical departments within the Shared Laboratory environment. Provides expertise and assistance for ... all clinical and non- clinical equipment (when able) and... equipment (when able) and supplies including coordinating product trials and monitoring contract compliance in order to assure… more
    Sutter Health (06/22/24)
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