• Summer 2026 - Legal - Graduate Intern

    Highmark Health (Pittsburgh, PA)
    …particular subject matter, market, and/or business segment. + Participating in the preparation of regulatory filings, document productions, investigation ... reviews and responses, pleadings reviews and responses, discovery requests and document productions, etc., and other matters, inquiries, and consults routinely… more
    Highmark Health (10/29/25)
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  • Nuclear Medicine/PET/CT Technologist - SRS Kearny…

    Sharp HealthCare (San Diego, CA)
    …on all nuclear medicine equipment. Procedures performed include preparation , administration, documentation and quality control of radiopharmaceuticals with ... of the Radioactive Materials License and all California State and Federal regulatory requirements. Assist staff with providing care to patients who have been… more
    Sharp HealthCare (12/13/25)
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  • Study Start Up Associate II - Oncology - San…

    ICON Clinical Research (NC)
    …forecasted timelines are at risk, and escalate issues as soon as identified. + Preparation , Submission, Review and Approval of Critical Document Package (CDP): + ... II** Responsibilities: + Collect, prepare, review, approve, process and track regulatory and site level critical documents required for study site activation… more
    ICON Clinical Research (11/21/25)
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  • Senior Financial Analyst - RPU

    The City of Rochester, MN (Rochester, MN)
    …conducts financial, statistical, and analytical studies; prepares and assists in the preparation of financial and regulatory reports, statements, and claims for ... *Budget Development/Monitoring + Develop the annual schedule for RPU budget preparation . + Coordinate the development of required budget model components by… more
    The City of Rochester, MN (12/11/25)
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  • Case Manager I - Transition Planner - Sharp…

    Sharp HealthCare (San Diego, CA)
    …position requires the ability to combine clinical/quality considerations with regulatory /financial/utilization review demands to assure patients are receiving care ... level of care.The RN CM I will recommend and document patient classification (status and level of care) for...CM I has accountability for maintaining compliance contractual and regulatory compliance with medical groups as applicable and the… more
    Sharp HealthCare (11/09/25)
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  • Per Diem RN - Case Management - Sharp Grossmont…

    Sharp HealthCare (La Mesa, CA)
    …position requires the ability to combine clinical/quality considerations with regulatory /financial/utilization review demands to assure patients are receiving care ... lower level of care.The RN CM will recommend and document patient classification (status and level of care) for...RN CM has accountability for maintaining compliance contractual and regulatory compliance with medical groups as applicable and the… more
    Sharp HealthCare (12/06/25)
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  • Senior Manager, Global HR Compliance

    PCI Pharma Services (Philadelphia, PA)
    …Operations, this role ensures that PCI's employment practices, including regulatory adherence, work authorization, policy management, government reporting, and ... programs, and the ability to operationalize HR policies and regulatory requirements across various systems, processes, and teams. **Responsibilities:** **Global… more
    PCI Pharma Services (12/09/25)
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  • Pharma Technical Writer

    System One (New Brunswick, NJ)
    …applications (Word, Excel, SharePoint, PPT) is required. + Experience with computer-assisted document preparation tools is preferred along with proficiency in ... should have at least 2 years of experience specifically for Regulatory CMC documentation within the pharmaceutical or biotechnology industry. Responsibilities +… more
    System One (09/23/25)
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  • Senior Clinical Research Director, Rare

    Sanofi Group (Cambridge, MA)
    …Clinical Study Units, and investigators + Develop the clinical part of Briefing regulatory documents, Common Technical Document for submission to regulatory ... leadership of the Global Project Head, with the Global safety Officer, Regulatory Strategist and other key functional representatives to deliver development strategy… more
    Sanofi Group (12/02/25)
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  • Development Scientific Director, I&I

    Sanofi Group (Morristown, NJ)
    …Study Units, and investigators + Contribute to the clinical part of Common Technical Document for submission to regulatory bodies (FDA, EMA, PMDA etc.) and ... leadership of the Global Project Head, with the Global safety Officer, Regulatory Strategist and other key functional representatives to deliver development strategy… more
    Sanofi Group (11/21/25)
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