• Supervisor, Clinical RN - Med/Surg Nursing…

    Guthrie (Sayre, PA)
    …support staff, exhibiting the Core Values in all activities. Mentors under the Clinical Manager / Director and pursues management and leadership training within ... Packer Hospital. May be assigned to special projects per Clinical Manager / Director consistent with strategic,...Supports the implementation of organization policies and procedures in compliance with state, Federal and other regulatory more
    Guthrie (09/18/25)
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  • Regulatory Coordinator

    University of Utah (Salt Lake City, UT)
    …patient care. **Preferences** A demonstrated understanding of human subjects research, regulatory documents, and quality compliance is strongly preferred. ... Details **Open Date** 08/19/2025 **Requisition Number** PRN42859B **Job Title** Regulatory Coordinator **Working Title** Regulatory Coordinator **Career… more
    University of Utah (08/20/25)
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  • Associate Director , Digital Health…

    Otsuka America Pharmaceutical Inc. (Des Moines, IA)
    …healthcare consulting, payer relations, or value-based care models. + Understanding regulatory and compliance requirements in healthcare engagement. + ... This is a high-autonomy, high-impact role that blends the best of on-label clinical education, access and reimbursement education, sales, and strategy - designed for… more
    Otsuka America Pharmaceutical Inc. (07/11/25)
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  • Director , WW HEOR Hematology - Multiple…

    Bristol Myers Squibb (Princeton, NJ)
    …and collaborate with hematology asset level matrix teams, including Value Access, clinical development, medical affairs, regulatory , biostatistics to ensure full ... alignment and integration HEOR evidence generation plan to support regulatory , Value Access/Pricing and brand strategic imperatives and objectives + Represent WW… more
    Bristol Myers Squibb (09/19/25)
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  • Director Patient Care - MS ICU

    Catholic Health Initiatives (Sugar Land, TX)
    …population that meets the standards of local, state, and national regulatory bodies and professional organizations. This position is responsible for providing ... in this position will assure the work environment adheres to regulatory requirements and departmental practices and processes reflect high quality standards… more
    Catholic Health Initiatives (08/14/25)
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  • Senior Principal Scientist, Clinical

    Merck (Upper Gwynedd, PA)
    clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. Specifically, the Senior Director may ... Our company's oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will manage the entire cycle… more
    Merck (09/04/25)
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  • Assistant Nurse Manager of Clinical

    Penn Medicine (Philadelphia, PA)
    …the Director , and members of the PTI leadership team to support clinical , quality, regulatory compliance , information systems, fiscal, and research goals ... satisfaction and concerns, electronic and medical record documentation processes Ensure Regulatory Compliance : In Partnership with Program leadership, ensure … more
    Penn Medicine (08/07/25)
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  • Head of Process and Drug Product Engineering…

    Genentech (Hillsboro, OR)
    …forefront of advancing cell and gene therapy medicines through accelerated clinical and commercial manufacturing capabilities, aligning with Genentech's mission to ... lifecycle management, and enable innovative, scalable systems that support ongoing clinical manufacturing as well as future commercial production. This role will… more
    Genentech (09/16/25)
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  • Senior Manager Regional Regulatory Lead…

    CSL Behring (King Of Prussia, PA)
    …and is onsite three days a week. You will report to the Executive Director Head Regulatory . **Position Description** **Summary** ** Regulatory leaders who ... worldwide. Could you be our next Senior Manager Regional Regulatory Lead, Hematology ? The job is in our... systems (** **e.g.** **Veeva) to ensure tracking and compliance deliverables.** **Applies the CSL Leadership Capabilities - Build… more
    CSL Behring (09/16/25)
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  • Senior Manager, Global Regulatory Affairs,…

    Takeda Pharmaceuticals (Boston, MA)
    Regulatory , Pharmaceutical Development, and Production project teams throughout clinical development and commercial lifecycle for assigned products and staff. ... Affairs CMC team, you will report to the Senior Director Global Regulatory Affairs CMC. **How you... submissions for assigned compounds in various phases of clinical development, global marketing applications, and post-approval life cycle… more
    Takeda Pharmaceuticals (07/08/25)
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