• Sr Human Subject Research Spec (H)

    University of Rochester (Rochester, NY)
    …Responsible for all aspects of clinical trial start-up oversight including protocol review, regulatory document preparation , and consent form preparation ... and submission to IRB. + Ensures maintenance of all human based study's regulatory records and subject study files. Oversees and participates in internal research… more
    University of Rochester (04/07/25)
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  • Regulatory Relations

    Mizuho Corporate Bank (New York, NY)
    …and ensure alignment on regulatory messaging. + Maintain up-to-date regulatory calendars, tracking tools, and document repositories to facilitate ... engagements + Participate in prep meetings and select regulatory interactions as appropriate, take notes, document ...action items + Conduct research and assist with the preparation of regulatory trend summaries, engagement trackers,… more
    Mizuho Corporate Bank (05/06/25)
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  • Senior Manager, Global Regulatory Affairs

    Otsuka America Pharmaceutical Inc. (Albany, NY)
    …working in the pharmaceutical and/or healthcare industry. - Knowledge and experience with preparation of global regulatory submissions (IND, CTA, NDA or BLA, ... **Position Summary** Provides critical support in developing global regulatory strategy, planning and execution of global investigational and marketed prescription… more
    Otsuka America Pharmaceutical Inc. (04/23/25)
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  • Temporary Document Services Representative

    CDPHP (Albany, NY)
    …values and invites you to be a part of that experience. The Document Service Representative shall assume full responsibility for the completion of the necessary ... are performed on-site. This includes performing a detailed mail sort, batch preparation , and scanning of all incoming claims and correspondence to facilitate and… more
    CDPHP (04/26/25)
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  • Senior Manager, CMC Global Regulatory

    Otsuka America Pharmaceutical Inc. (Albany, NY)
    Provide CMC regulatory strategy input and expertise in the area of investigational, new and marketed biologic and small molecule drug products to assigned project ... ensure Otsuka's products are developed/maintained in compliance with global regulatory requirements and guidances. Primary regions/markets of responsibility include… more
    Otsuka America Pharmaceutical Inc. (04/26/25)
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  • Global Markets Non-Financial Regulatory

    Bank of America (New York, NY)
    …of Laws, Rules and Regulations (LRRs) and Enterprise Policies, data sourcing, preparation , governance, and oversight of Global Markets regulatory reports - ... Global Markets Non-Financial Regulatory Reporting (GM NFRR) Operational Monitoring New York,...accurate data foundation that captures key metrics for report preparation process into a source of actionable information. Regularly… more
    Bank of America (04/12/25)
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  • Regulatory Compliance Senior Associate

    Grant Thornton (New York, NY)
    As a Regulatory Compliance Risk Senior Associate, you will get the opportunity to grow and contribute to our banking clients' business needs by providing in-depth ... emerging regulations and help organizations leverage efficiencies within the Risk, Regulatory Compliance & Controls Practice - all with the resources, environment,… more
    Grant Thornton (04/23/25)
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  • Environmental Specialist 2 (Nyhelps)

    New York State Civil Service (Long Island City, NY)
    …the project development process, especially those made in the Design Approval Document , to make sure the Department is meeting the FHWA's requirements.* Manage ... on environmental matters when interacting with federal and state environmental regulatory agencies and groups.* Provide leadership and guidance on environmental… more
    New York State Civil Service (05/10/25)
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  • Medical Writer II

    ICON Clinical Research (New York, NY)
    …at ICON, you will play a pivotal role in the development and preparation of clinical trial documents, regulatory submissions, and scientific publications, ... (CSRs), clinical protocols, investigator brochures (IBs), patient narratives, and other regulatory documents in compliance with internal standards and regulatory more
    ICON Clinical Research (04/17/25)
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  • Standards Analyst

    City of New York (New York, NY)
    …To operate an effective capital program, construction specifiers must understand document organization, document preparation and contractual relationships ... new ones based on either established Agency business practices, new regulatory requirements or independent research of industry best practices. BEDC delivers… more
    City of New York (04/26/25)
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