• Clinical Research Assistant II Regulatory…

    Mount Sinai Health System (New York, NY)
    …and study specific regulatory binders for all studies. **Document Collection and Review ** : + Collaborate with regulatory affairs team to collect required ... **Job Description** The Regulatory Assistant II plays a vital role in...Review documents for completeness, accuracy, and compliance with regulatory standards. + Identify and rectify any errors or… more
    Mount Sinai Health System (08/08/25)
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  • Analyst, Medicaid Compliance

    CVS Health (Oklahoma City, OK)
    …+ Prepares routine regulatory reports, filings, and follow-ups, and supports regulatory review and audit activities. + Contributes to an effective compliance ... programs and processes that promote compliant and ethical behavior, meet regulatory obligations and prevent, detect, and mitigate compliance risks. **Job… more
    CVS Health (10/19/25)
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  • Clinical Research Specialist

    University of Pennsylvania (Philadelphia, PA)
    …regulatory documentation through the IRB, FDA and all applicable institutional regulatory review committees. In collaboration with clinical research teams and ... Temporary Employee - Non-Exempt Job Description Ophthalmology seeks a part-time Regulatory Affairs Start-Up Specialist-CC to facilitate, with minimal supervision ,… more
    University of Pennsylvania (08/03/25)
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  • Access Service Representative-Patient Focus…

    Sharp HealthCare (La Mesa, CA)
    …initiate Health Information Exchange (HIE) process as appropriate.In areas performing post regulatory review , address outstanding alerts in the Centricity Alerts ... Tricare or Medicare/Medicare Advantage is primary or secondary, use scripting to review and deliver appropriate regulatory form (Tricare Rights, Tricare Third… more
    Sharp HealthCare (10/31/25)
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  • Director Of Regulatory Affairs

    Actalent (Maryland Heights, MO)
    … regulatory governmental policy changes to management. + Critically review documentation for regulatory submissions and provide necessary revisions. ... Director of Regulatory Affairs The Director of Regulatory Affairs is tasked with overseeing Nuclear Medicine Regulatory Affairs dossiers and ensuring… more
    Actalent (10/25/25)
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  • Regulatory Affairs Manager - JC

    Pedernales Electric Cooperative (Johnson City, TX)
    …position through participation in the stakeholder processes. + Perform a substantive review of applicable regulatory and policy issues, including when ... Regulatory Affairs Manager - JC Johnson City, TX,...responsible for supporting strategies and operations of the organization's regulatory affairs function, which ensures compliance with governmental regulations… more
    Pedernales Electric Cooperative (10/16/25)
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  • Associate Director, Regulatory Affairs…

    Sumitomo Pharma (Lincoln, NE)
    …documentation to Health Authorities + Assist with development of the global regulatory functional plan through research, review and interpretation of related ... highly motivated, and experienced individual for the position of **Associate Director, Regulatory Affairs (Oncology).** The Associate Director is part of the Global … more
    Sumitomo Pharma (10/11/25)
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  • Senior Regulatory Counsel

    ITG Brands (NC)
    …with regulatory agencies, industry groups, and external counsel. Draft, review , and negotiate regulatory -related agreements and documents. Educate and advise ... Senior Regulatory Counsel **Location** North Carolina **City** Greensboro **Role...+ We are seeking a seasoned and strategic Senior Regulatory Counsel to join our Legal and Regultaory team.… more
    ITG Brands (09/30/25)
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  • Water Systems Analyst, Bureau of Environmental…

    City of New York (New York, NY)
    …reports related to the program's compliance and surveillance activities, study findings, regulatory review of the City's drinking and recreational water quality ... or environmental health. - Experience in engineering plan and specification review , regulatory enforcement, environmental investigations, water treatment, or… more
    City of New York (08/13/25)
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  • Medical Director, Medical Device, Patient Safety

    AbbVie (North Chicago, IL)
    …Assessments and Health Hazard Evaluations + Contribute to writing safety responses to regulatory authorities + Review literature to support submission of new ... collaboration with cross-functional teams and counterparts in quality systems, regulatory affairs, medical writing, clinical development, clinical operations, manufacturing,… more
    AbbVie (10/26/25)
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