• Summer Intern PhD Student - Chemical…

    Bristol Myers Squibb (New Brunswick, NJ)
    …and in their personal lives. Read more: careers.bms.com/working-with-us . Chemical Process Development (CPD) is a team of organic chemists, analytical chemists, and ... the manufacturing process, design parameters, and control strategies enables regulatory filings to bring these novel medicines to patients...work with mentors for ~10 weeks on a guided research project within a CPD Project Team. The program… more
    Bristol Myers Squibb (11/08/25)
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  • 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 (10/08/25)
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  • Associate Principal Scientist, Biologics…

    Merck (Rahway, NJ)
    **Job Description** **Associate Principal Scientist, Biologics Analytical Research & Development ** Our Research Scientists are our Inventors. We identify and ... methodology, we collaborate to discover the next medical breakthrough. The Biologics Analytical Research & Development department of our Research & … more
    Merck (11/05/25)
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  • Associate Director, Regulatory Liaison…

    Merck (Rahway, NJ)
    regulatory lead. + Conducting research and review of guidelines, regulatory precedence and competitive intelligence to facilitate development of ... Strategy, Innovation, Regulatory Affairs Management, Regulatory Strategy Development , Regulatory Submissions, Scientific Research , Strategic Thinking… more
    Merck (11/21/25)
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  • Director Global Regulatory Strategy…

    Bayer (Whippany, NJ)
    …Strategy (Molecular Imaging, Pharmaceuticals)** The position is responsible for the development , alignment, and implementation of regulatory strategies to ensure ... in charge for assessing and aligning the probabilities for regulatory success for the assigned development programs....a BS degree is required; + Experience in biomedical research , including local/global regulatory experience in related… more
    Bayer (11/25/25)
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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 (09/23/25)
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  • VP, Regulatory Affairs R&D Biopharma

    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 ... Regulatory matters in close partnership with the Chief Development Officer and other key stakeholders + Establish key...to late-stage investigational assets, we aim to accelerate discovery, research , and development to bring novel therapies… more
    Sumitomo Pharma (09/10/25)
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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 (11/19/25)
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  • Senior Principal Scientist, Clinical…

    Merck (Rahway, NJ)
    …study reports, or publication; and + Participation in internal and joint internal/external research project teams relevant to the development of new compounds ... regulatory affairs, statistics, and manufacturing to manage clinical development projects; and assist the Executive Director in ensuring that appropriate… more
    Merck (11/22/25)
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  • Associate Principal Scientist, Regulatory

    Organon & Co. (Jersey City, NJ)
    …+ Lead development and execution of global product and project regulatory strategy(ies) by ensuring robust assessment of CMC changes, identification of global ... documentation to confirm acceptability and identification of potential risks. + Execute regulatory strategies by leading the development , authoring and review of… more
    Organon & Co. (10/24/25)
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