• Associate Director, Global Publications

    Gilead Sciences, Inc. (Foster City, CA)
    …create strategic annual publication plans and publish high-impact scientific and medical data + Work cross-functionally with subject matter experts across all ... data -generating functions (including, but not limited to, Clinical Development,...and multiple myeloma + Work independently to prioritize, execute, review , and edit key tactics consisting of congress abstracts… more
    Gilead Sciences, Inc. (06/26/25)
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  • Staff Analog Circuit Design Engineer

    Teledyne (Milpitas, CA)
    …research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research.​ We are looking for individuals who thrive on making an ... measured performance and compare to design goals, and to review and guide PCB layout to ensure analog circuitry...analog circuits for probing and amplifying high speed serial data :** + Design high speed amplifier subsystems using off… more
    Teledyne (06/13/25)
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  • Senior Associate General Counsel- US Litigation…

    Gilead Sciences, Inc. (Foster City, CA)
    …expert witness work, and preparation for key hearings and trial. Review correspondence, arguments, memos, and briefs in support of litigation, investigations ... Gilead. + Advance innovation and efficiency by leveraging legal technology and data analytics to improve efficiency in case management, drive cost containment, and… more
    Gilead Sciences, Inc. (06/11/25)
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  • Clinical Research Coordinator I, Laboratory…

    Cedars-Sinai (Los Angeles, CA)
    …subjects, clinic and research staff, laboratory staff, medical professionals, pharmaceutical staff, and Sponsor representatives to successfully implement research ... compliance and patient safety. + Responsible for accurate and timely data collection, documentation, entry and reporting, including timely response to sponsor… more
    Cedars-Sinai (06/07/25)
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  • Principal Regulatory Affairs Specialist - Vascular…

    Abbott (Santa Clara, CA)
    …role by partnering across business functions. The individual may assist in identifying data needed, obtaining these data , and ensuring that they are effectively ... preclinical and clinical documentation for submission filing. + Compile, prepare, review and submit regulatory submissions to authorities. + Monitor impact of… more
    Abbott (08/29/25)
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  • RayzeBio Associate Director - Biostatistical…

    Bristol Myers Squibb (San Diego, CA)
    …documents, and other internal ad-hoc requests + Collaborate with cross-functional teams to review critical study documents and perform data reviews for ongoing ... the following. Other duties may be assigned. + Oversee vendors' activities, and review vendors' deliverables to ensure quality + Create/QC SDTM/ADaM data more
    Bristol Myers Squibb (08/30/25)
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  • Customer Success Manager

    Datavant (Sacramento, CA)
    …a case-by-case basis. For more information about how we collect and use your data , please review our Privacy Policy (https://www.datavant.com/privacy-policy) . ... Datavant is a data platform company and the world's leader in...sector + Application of RWD and RWE in the pharmaceutical and life sciences space + Understanding of drug… more
    Datavant (07/31/25)
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  • Sr. Director, Clinical Development (MD)-…

    Gilead Sciences, Inc. (Foster City, CA)
    …to assessment of eligibility criteria, addressing investigator questions, safety monitoring, and ensuring high data quality through data review as part of a ... inquiries + Provide scientific and clinical leadership or oversight in the preparation, review , and interpretation of clinical study data , ensuring high quality … more
    Gilead Sciences, Inc. (07/24/25)
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  • Director, Gher Tmtt Real World Evidence

    Edwards Lifesciences (Irvine, CA)
    …planning, execution, and oversight of real-world evidence generation using real-world data (RWD) to identify patient unmet needs, overcome market access barriers, ... analytic plans for assigned studies. + Direct the development and execution of data management plans across various relational databases, with proficiency in data more
    Edwards Lifesciences (08/16/25)
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  • Clinical Research Coordinator III - Guerin…

    Cedars-Sinai (Los Angeles, CA)
    …agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). **What are the Primary Duties & Responsibilities?** + ... related to all research procedures. + Responsible for accurate and timely data collection, documentation, entry, and reporting including timely response to sponsor… more
    Cedars-Sinai (08/01/25)
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