• Biomedical Data Stewardship Senior Manager

    Amgen (Thousand Oaks, CA)
    …designation and definition of standard, indication-level CRF libraries using global standards-based and study-specific content and document implementation rules and ... conducting audits and reviews to ensure alignment with evolving study and regulatory needs. + Manage governance processes for evaluating and implementing updates or… more
    Amgen (06/27/25)
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  • VP Compliance, US Core Control Room (San Francisco…

    TD Bank (San Francisco, CA)
    …and respond to conflicts clearance requests, and work through questions from the global Control Room inbox. + Review and escalate conflict checks for the Investment ... Bank. + Participate in regulatory exams and work with internal auditors. + Participate...providing trusted advice and industry-leading insight, extending access to global markets, and delivering integrated transaction banking solutions. In… more
    TD Bank (08/16/25)
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  • Late

    Pfizer (South San Francisco, CA)
    …contributes to authoring of IBs, site training materials, clinical study reports, regulatory responses, and other clinical and regulatory documents; supports ... clinical procedures, ICH guidelines, GCP and familiarity with FDA, EMA, and global regulations. + Strong scientific writing skills and communication skills (written… more
    Pfizer (08/15/25)
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  • Director, Patient Services and HUB

    Sumitomo Pharma (Sacramento, CA)
    Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the US (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma ... and market access goals. + Collaborate closely with **legal, compliance, privacy and regulatory teams** to ensure program design and execution adheres to all. +… more
    Sumitomo Pharma (08/15/25)
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  • Vice President, Government Relations

    Allied Universal (Irvine, CA)
    …Universal(R) is hiring a Vice President, Government Relations. Allied Universal(R), a global leader in security and facility services, is seeking a Vice President ... and based at our corporate headquarters In Irvine, CA. Reporting to the Global Chief Communications & Investor Relations Officer (with a dotted-line to the… more
    Allied Universal (08/13/25)
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  • Analyst, Tech Controls

    Coinbase (Sacramento, CA)
    …day, as we build the emerging onchain platform - and with it, the future global financial system. To achieve our mission, we're seeking a very specific candidate. We ... IT process and gap assessments against industry standards and technology regulatory requirements to evaluate control design and operating effectiveness * Design,… more
    Coinbase (08/09/25)
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  • Project Manager I

    Charles River Laboratories (Northridge, CA)
    …multiple high-impact projects simultaneously. Experience in client communication, regulatory environments, and process improvement is highly desirable. Essential ... workflows. + Collaborate with departments such as R&D, Quality, Regulatory , and Manufacturing to meet project goals. + Ensure...River Cell Solutions** Charles River Cell Solutions is a global leader and trusted brand in the customization of… more
    Charles River Laboratories (08/08/25)
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  • Environmental Health and Safety Consultant

    Stantec (Roseville, CA)
    …and studies, including environmental remediation and restoration. + EHS regulatory compliance assessments and audits at industrial and manufacturing client ... and/or state environmental regulations. + Technical consulting for clients on regulatory compliance matters including permit management, routine regulatory more
    Stantec (08/07/25)
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  • Principal Supplier Quality Engineer, Selution

    Cordis (Irvine, CA)
    …of people and broadening access to life-saving cardiovascular and endovascular technology. As a global leader for over 60 years, we are dedicated to being the heart ... teammates are inspired to unleash their full potential. With diverse teams on a global scale, we believe the richness of our experiences and backgrounds enhances the… more
    Cordis (07/29/25)
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  • Late Stage Oncology Clinical Scientist

    Pfizer (San Francisco, CA)
    …contributes to authoring of IBs, site training materials, clinical study reports, regulatory responses, and other clinical and regulatory documents; supports ... clinical procedures, ICH guidelines, GCP and familiarity with FDA, EMA, and global regulations. + Strong scientific writing skills and communication skills (written… more
    Pfizer (07/26/25)
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