• Communications Specialist II, Scientific…

    University of Rochester (Rochester, NY)
    …wide range of scientific and medical documents in support of clinical, regulatory , and collaborative functions across CHeT. Ensures accuracy, clarity, and alignment ... therapeutic areas, while maintaining compliance with medical writing standards and regulatory requirements. **ESSENTIAL FUNCTIONS** + Develops and authors a variety… more
    University of Rochester (08/10/25)
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  • Vice President, Global Patient Safety Operations

    Regeneron Pharmaceuticals (Tarrytown, NY)
    …operations, quality and compliance, planning, and assessing and implementing regulatory requirements, along with shown capabilities to lead cross-functional ... objectives and applicable initiatives on behalf Regeneron's portfolio and regulatory requirements. + Provide pharmacovigilance leadership, expertise and guidance to… more
    Regeneron Pharmaceuticals (06/03/25)
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  • Market Risk Stressed RWA Modelling

    SMBC (New York, NY)
    …and support various workstreams which will be responsible for calculating the bank's regulatory capital of trading book portfolios. This role will have a high level ... solid grasp of financial markets as well as US regulatory framework. **Role Objectives** + Lead the development of...a related field is required. Advanced degree (MS or PhD ) is highly desirable. + Minimum of 5 years… more
    SMBC (05/20/25)
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  • Sr Director, Medical Evidence Generation Asset…

    Pfizer (New York, NY)
    …all relevant stakeholders (eg, Medical Affairs, Epidemiology/RWE, Statistics/Programming, Regulatory , Safety, Operations, Quality, Global Access & Value, ... deliverables + Act as MEG asset reviewer for critical regulatory and select study-level documents as needed + Represent...medical affairs colleagues **Qualifications** + Advanced degree (PharmD, MD, PhD , or equivalent) with 7+ years, MS with 10+… more
    Pfizer (08/15/25)
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  • Director Quantitative Pharmacology

    Regeneron Pharmaceuticals (Tarrytown, NY)
    …the most complex situations. . Informs PMx management of important program and regulatory developments in a timely manner. . Ensures analyses and documentation are ... in own area within the organization. . Have extensive regulatory experience through authoring of regulatory briefing...considered qualified for this role,** you must have a PhD +8 years with a degree in Quantitative Pharmacology… more
    Regeneron Pharmaceuticals (06/27/25)
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  • Lead HPC Architect Cybersecurity - High…

    Mount Sinai Health System (New York, NY)
    …we support a cutting-edge high-performance computing and data ecosystem along with MD/ PhD -level support for researchers. The group is composed of a high-performance ... degree in computer science, engineering or another scientific field. Master's or PhD preferred. + 10 years of progressive HPC system administration experience with… more
    Mount Sinai Health System (08/14/25)
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  • Oncology Early Stage Clinical Scientist Senior…

    Pfizer (New York, NY)
    …supports other critical documents, eg, protocol amendments, investigator brochure, and regulatory documents. + Collaborate with Clinical Operations to ensure timely ... strategy and/or data, and may assist with authoring clinical sections of regulatory documents (IB, Annual Reports, IND sections, CSR). + Support and assists… more
    Pfizer (08/15/25)
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  • Executive Medical Director, Clinical Development,…

    Regeneron Pharmaceuticals (Tarrytown, NY)
    …submission/approval of a clinical development program to support decision milestones and regulatory requirements. This role is a clinical subject matter expert for ... compound. + Leads creation of clinical components of key documents ( regulatory documents, registration dossiers, etc.) supporting registration, market access, and… more
    Regeneron Pharmaceuticals (08/15/25)
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  • Global Development Lead, Medical Director,…

    Pfizer (New York, NY)
    …investigator brochures, clinical study reports, statistical analysis plan, and regulatory documents. + Provide leadership to early stage clinical scientists ... with other clinicians, statisticians, clinical pharmacologists, translational biologists and regulatory specialists. Meet regularly with the Pfizer Oncology group… more
    Pfizer (08/08/25)
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  • Model Risk Management - Credit Model Validation…

    Citigroup (Queens, NY)
    …term structure model is preferred. A firm understanding of model risk management regulatory guidance SR 11-7 as it relates to effective model validation practices is ... to work well with senior stakeholders within the firm and with our regulatory colleagues is essential. This role has high visibility and growth potential--clear… more
    Citigroup (07/30/25)
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