• Statistics Intern ( PhD )

    AbbVie (Florham Park, NJ)
    …business decisions. The team works collaboratively with other departments across clinical development , regulatory affairs, and global medical affairs to provide ... support for various projects and initiatives across all phases of clinical development . The Stats organization is composed of highly skilled statisticians, data… more
    AbbVie (01/07/26)
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  • Research Scientist Analytical…

    Bayer (Morristown, NJ)
    …and diverse minds to make a real difference, there's only one choice.** ** Research Scientist Analytical Development ** **Position Overview:** As an Analytical ... at the forefront of designing analytical experiments to drive new product development for global markets. Your role involves developing, validating, and transferring… more
    Bayer (12/08/25)
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  • Vice President, Regulatory Affairs…

    Sumitomo Pharma (Trenton, NJ)
    …a diverse pipeline of early- to late-stage assets, we aim to accelerate discovery, research , and development to bring novel therapies to patients sooner. For ... HTA submissions. The individual will be responsible for leading development of all non-clinical and clinical regulatory ...the Marketing Brand Teams, Legal, Medical Affairs and Clinical Research in the development of advertising and… more
    Sumitomo Pharma (12/23/25)
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  • Principal Scientist, Medical Device Expert,…

    L'Oreal USA (Clark, NJ)
    …& Innovation Full - Time 09-Jan-2026 Principal Scientist, Medical Device Expert, Research & Innovation, Safety Evaluation, Regulatory Affairs and Claims ... as a key interface with Asia Pacific and European hubs. Provide regional regulatory requirements and technical guidance to product development teams and to… more
    L'Oreal USA (01/12/26)
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  • Senior Principal Scientist, Clinical…

    Merck (Rahway, NJ)
    …Curiosity, Interdisciplinary Problem Solving, Neuropathic Pain, Neuroscience, Neuroscience Research , Pain Management, Pharmaceutical Development , Regulatory ... development , including study design, initiation, execution, monitoring, analysis, regulatory reporting, publication, and presentation at national and international… more
    Merck (01/10/26)
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  • Director, Early Precision Medicine…

    Bristol Myers Squibb (Princeton, NJ)
    …scientific background, PhD ., MD, PharmD, MS + Significant experience in regulatory affairs and diagnostic-related development eg, >8-10 years. + Scientific & ... risk mitigation planning. + Cultivate inclusive, high-impact collaboration with Precision Medicine, Research teams, Global and Regional Regulatory Leads, Global … more
    Bristol Myers Squibb (12/03/25)
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  • Head of Global Regulatory Affairs, CMC…

    Sanofi Group (Morristown, NJ)
    …across the product lifecycle. Our department bridges the gap between technical development , manufacturing operations, and global regulatory authorities to ensure ... and behaviors that model the Sanofi and GRA Values/Principles/Competencies. + Oversees the development of CMC regulatory strategy and regulatory risk… more
    Sanofi Group (12/22/25)
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  • Senior Director, Global Regulatory Lead…

    Bristol Myers Squibb (Princeton, NJ)
    …be a key member of the GRSP Extended Leadership Team to ensure the development , implementation, and alignment of regulatory strategies across projects and the ... various company-wide projects and initiatives. + Support due diligence and business development assessments. + Working with regional regulatory staff as Global… more
    Bristol Myers Squibb (01/02/26)
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  • Associate Director, Health Economics & Outcomes…

    Otsuka America Pharmaceutical Inc. (Princeton, NJ)
    …for conferences, corporate locations, and stakeholder meetings. Educational Qualifications: + PhD or Masters in Health Economics, Outcomes Research , Health ... Services Research , Public Health or related discipline + Three ( PhD ) to five (Masters) years of relevant experience **Competencies** **Accountability for Results… more
    Otsuka America Pharmaceutical Inc. (12/20/25)
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  • Senior Director, Clinical Research

    Merck (Rahway, NJ)
    development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director May Be ... study reports, or publication + Participation in internal and joint internal/external research project teams relevant to the development of new compounds,… more
    Merck (01/10/26)
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