• 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 (07/13/24)
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  • Live Support, Clinical Research Operations…

    Stanford University (Stanford, CA)
    …Research Operations Specialist II to conduct and manage a large multi-site clinical trial . Research will be conducted in cardiovascular medicine. The ... Live Support, Clinical Research Operations Specialist II (REACT)...for promoting/recruiting research participants and retaining participants in long-term clinical trials . + Oversee data management for… more
    Stanford University (07/10/24)
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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 (08/14/24)
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  • Manufacturing Specialist

    Stanford University (Stanford, CA)
    …disease and the promotion of health in pediatric and adult patients in Phase I/II clinical trials . The person hired for this role will join a Process Development ... focused on manufacturing cell products for the phase I/II clinical trials supported by Stanford investigators or...current Good Manufacturing Practice (cGMP) and aligned with the clinical trial investigational phase for treating patients… more
    Stanford University (08/21/24)
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  • Senior Clinical Pharmacologist - Virology,…

    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. (08/31/24)
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  • Capital Technical Support Specialist

    AbbVie (Pleasanton, CA)
    …order types: EDI, fax, email, phone, for RX, OTC, control drugs, clinical trials , serialized products, including vaporizers and pumps. Support establishment ... Clear and Courageous, Make Possibilities Real + Complete/apply all quality, regulatory safety, and compliance training + Support audit documentation requirements for… more
    AbbVie (09/20/24)
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