• Senior Vice President, Global Development…

    Bristol Myers Squibb (Princeton, NJ)
    …Operations function, accountable to lead an integrated, end to end global clinical operations function accountable for acceleration and delivery of clinical ... vision for the function and in the execution of clinical trials + Manages, builds and leads global development...goals in compliance with GCP, ICH and other global regulatory requirements + Provides comprehensive strategic leadership for 2,100+… more
    Bristol Myers Squibb (11/25/25)
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  • Biomedical Equipment Support Specialist…

    Veterans Affairs, Veterans Health Administration (Grand Junction, CO)
    …safety, cybersecurity, and decommissioning. They plan, implement, and provide technical and project oversight for medical equipment and clinical systems. BESSs ... medical servers and networks, diagnostic software, virtual platforms, and clinical applications software. Responsibilities Manages and maintains medical servers and… more
    Veterans Affairs, Veterans Health Administration (11/19/25)
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  • Assistant Chief Medical Officer, Hospital

    Intermountain Health (St. George, UT)
    …and ensure compliance with laws and external agencies regarding accreditation and regulatory bodies affecting clinical practice. + Proactively support efforts to ... Lean, Project Management, Advanced Training Program). Significant portion of clinical work done within the hospital setting. Experience working in a complex… more
    Intermountain Health (10/31/25)
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  • Informaticist RN

    Catholic Health Initiatives (Houston, TX)
    **Job Summary and Responsibilities** Responsible for advancing clinical practice and improving patient outcomes through the effective integration and utilization of ... Clinical Information Systems (CIS) in the practice environment. Assist...efforts including, but not limited to quality and or regulatory requirements. 11. Analyze issues and develop recommendations with… more
    Catholic Health Initiatives (10/24/25)
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  • Quality Assurance/Improvement Specialist

    State of Montana (Helena, MT)
    …include, but not limited to: Ensuring compliance with laboratory accreditation and regulatory standards; Recommending best practices to improve project outcomes ... Five years of related laboratory work experience such as high complexity clinical laboratories, environmental laboratories, and research laboratories. o Must be… more
    State of Montana (11/19/25)
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  • Associate Director, Scientific Communications…

    Takeda Pharmaceuticals (Boston, MA)
    …coordination with relevant cross-functional teams (including members of medical affairs, clinical development, and outcomes research ; global, regional, or ... and analytical background, preferably in life sciences, and excellent project management skills. The Associate Director, Scientific Communications Lead, develops… more
    Takeda Pharmaceuticals (09/11/25)
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  • Director of Surgical Marketing

    Edwards Lifesciences (Irvine, CA)
    …of marketing messages based on regional strategies, deep knowledge of clinical data, products, current literature, current competitive environment, and regulatory ... marketing collateral and labeling through all relevant legal and regulatory approval processes through collaboration with relevant marketing partners and… more
    Edwards Lifesciences (11/04/25)
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  • Senior Counsel, Digital

    GE HealthCare (Chicago, IL)
    …and complex transactions, including technology licensing, data and analytics, clinical & research partnerships, business development, software development, ... outbound technology licensing, software development, cloud deployment, professional services, and clinical and research partnerships. + Design and conduct strong… more
    GE HealthCare (11/19/25)
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  • Life Sciences Specialist Leader

    Deloitte (Princeton, NJ)
    …clients within the Life Sciences & Healthcare sector, utilizing Veeva Vault Clinical Trial Management Systems (CTMS), Regulatory Information Management ( RIM) ... and delivery while managing risks and quality of delivery, utilizing Veeva Vault Regulatory Information Management ( RIM) Suite , Clinical Suite, Clinical more
    Deloitte (11/14/25)
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  • Principal Human Factors Engineer

    Genentech (South San Francisco, CA)
    …devices. They will collaborate with multifunctional teams including device engineering, regulatory , clinical , quality, marketing, and program management to ... and easy to use. The candidate has demonstrated ability to lead project -level human factors activities, including ethnographic research , requirements definition … more
    Genentech (11/11/25)
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