• Senior Director, Global Media Relations

    Gilead Sciences, Inc. (Parsippany, NJ)
    …team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve ... serve as a key advisor and collaborator with key business partners (Public Affairs , Investor Relations, Government Affairs , and other functions) to formulate and… more
    Gilead Sciences, Inc. (09/05/25)
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  • Director, Global Medical Oncology, US IO Lung…

    Bristol Myers Squibb (Princeton, NJ)
    …Medical launch plans and life cycle management plans. + Provide strategic, scientific , and executional leadership while partnering with the integrated matrix team, ... and implement key medical activities, including medical advisory boards, Scientific Engagement Partner resources and training, congresses, reactive content, and… more
    Bristol Myers Squibb (10/02/25)
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  • Global Medical Director - Hemophilia

    Sanofi Group (Morristown, NJ)
    …+ Accountable for implementing stakeholder engagement, medical education, and scientific communication plans aligned with the strategic priorities of the ... and cross-functional teams. + Deploy innovative tools and channels for scientific communication and data dissemination, such as omnichannel and AI-based approaches.… more
    Sanofi Group (09/12/25)
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  • R&D Regulatory Manager

    Grifols Shared Services North America, Inc (Trenton, NJ)
    …ensure alignment of technical activities with regulatory strategies. + Utilizes scientific training when interfacing with Management of technical areas and project ... around emerging/changing regulatory requirements. + Writes documents with complex scientific information for regulatory submissions. + May supervise staff +… more
    Grifols Shared Services North America, Inc (08/01/25)
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  • Senior Regulatory Specialist, Data Management…

    Cardinal Health (Trenton, NJ)
    **_What Regulatory Affairs contributes to Cardinal Health_** Regulatory provides regulatory affairs and product development consulting services to enable ... as well as clinical research and manufacturing process consulting. Regulatory Affairs plans, coordinates and implement regulatory strategies for products that… more
    Cardinal Health (10/10/25)
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  • Director, Global Real World Evidence (RWE)…

    J&J Family of Companies (Raritan, NJ)
    …closely with GCDS verticals and cross-functional teams, including Global Medical Affairs , Global Market Access, Global Marketing, Global Epidemiology, J&J Technology ... Data Sciences, R&D Data Science, and regional medical affairs and evidence generation partners. Responsibilities may evolve in...in the conduct of RW Research and dissemination of scientific information. + Lead the coordination and execution of… more
    J&J Family of Companies (10/07/25)
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  • Global Medical Evidence Generation Lead…

    Sanofi Group (Morristown, NJ)
    …that is part of the Global Rare Disease Medical Team. Our Medical Affairs function serves as a key strategic partner with commercial, regulatory, clinical, HEVA ... needed + Lead the execution and support the strategy of global Medical Affairs studies, including the management of the study Steering Committee, development of the… more
    Sanofi Group (09/11/25)
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  • Director, Medical Strategy, Global Medical…

    Bristol Myers Squibb (Princeton, NJ)
    …concept through full execution, including reporting the evidence at scientific congresses, in peer reviewed publications, and proactive/reactive BMS communication ... manner + Attends major conferences and helps coordinate medical affairs activities at conferences + Responsible for the development...to questions in response to issues relative to commercial, scientific , or data needs + Serves as medical strategy… more
    Bristol Myers Squibb (10/11/25)
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  • Associate Principal Scientist, Clinical Research…

    Merck (Rahway, NJ)
    …of paper and Electronic Data Capture (EDC) clinical studies that meet scientific and regulatory requirements by the setting of objectives, budget, resources, ... Study Report + Maintain contact with all stakeholders (project leader, regulatory affairs , quality assurance etc.) and keeps them informed of the study progress.… more
    Merck (10/09/25)
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  • Director, Clinical Pharmacology Lead

    Organon & Co. (Jersey City, NJ)
    …modeling vendors) colleagues. The Clinical Pharmacology Lead will ensure the scientific and clinical pharmacology components of study protocols are sound, based ... colleagues in preclinical science, data science, clinical operations, regulatory affairs , chemistry, manufacturing and control (CMC), project management and other… more
    Organon & Co. (10/02/25)
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