• Associate Principal Scientist

    Organon & Co. (Jersey City, NJ)
    …questions per established business processes and systems. + Demonstrate an understanding of regulatory affairs and apply this understanding to the benefit of the ... **The Position ** Reporting to the Director in Organon Regulatory CMC, the Associate Principal Scientist is...in Organon Regulatory CMC, the Associate Principal Scientist is responsible for developing and implementing Regulatory more
    Organon & Co. (10/24/25)
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  • Sr. Scientist II - Regulatory

    Mondelez International (East Hanover, NJ)
    …; Know Your Rights: Workplace Discrimination is Illegal **Job Type** Regular Scientific Affairs & Regulatory Affairs Product Quality, Safety and Compliance ... Future of Snacking. Make It With Pride.** The Sr. Scientist II will execute the Scientific Affairs ...respective categories and geographical area using your Scientific and Regulatory expertise. You advocate for our regulatory more
    Mondelez International (10/24/25)
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  • Senior Principal Scientist , Translational…

    Merck (Rahway, NJ)
    …scientists (including discovery research, biostatistics, drug metabolism, modeling and simulation, regulatory affairs , and global clinical trials operations) + ... Translational Medicine Operations, Translational Medicine-EU, Drug Metabolism/Modeling & Simulation, Regulatory Affairs , and late-stage Clinical Research throughout… more
    Merck (12/03/25)
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  • Senior Principal Scientist , Clinical…

    Merck (Rahway, NJ)
    …teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs, vaccines and new indications for existing ... medicines, and we work with cross-functional colleagues in Global Medical and Scientific Affairs and Global Policy to ensure timely and equitable access to our… more
    Merck (12/02/25)
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  • Associate Principal Scientist , Clinical…

    Merck (Rahway, NJ)
    …the Final Study Report + Maintain contact with all stakeholders (project leader, regulatory affairs , quality assurance etc.) and keeps them informed of the ... include but are not limited to:_ The Associate Principal Scientist is a DVM and/or PhD whose primary function...clinical laboratory and field studies that will support the regulatory approval of new companion animal and livestock products.… more
    Merck (12/04/25)
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  • Senior Principal Scientist , Clinical…

    Merck (Rahway, NJ)
    …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... Neuropathic Pain, Neuroscience, Neuroscience Research, Pain Management, Pharmaceutical Development, Regulatory Affairs Compliance, Regulatory Compliance,… more
    Merck (12/02/25)
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  • Senior Principal Scientist , Clinical…

    Merck (Rahway, NJ)
    …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... **Job Description** The Senior Director (Sr. Principal Scientist ) has primary responsibility for the strategic planning and directing clinical research activities… more
    Merck (12/02/25)
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  • Principal Scientist , Clinical Research,…

    Merck (Rahway, NJ)
    …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... **Job Description** The **Clinical Director (Principal Scientist )** has primary responsibility for the strategic planning and directing clinical research activities… more
    Merck (12/02/25)
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  • Associate Director, Medical Omnichannel Data…

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …access to treatment. We are looking for an **Omnichannel Data Scientist ** , **Medical Omnichannel** with strong expertise in artificial intelligence, encompassing ... to address strategic objectives to business partners. + Work closely with medical affairs , marketing, and IT teams to ensure alignment and integration of omnichannel… more
    Otsuka America Pharmaceutical Inc. (12/03/25)
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  • Senior Clinical Trial Physician, Rheumatology

    Bristol Myers Squibb (Madison, NJ)
    …of key functions (eg, early development, TM, clinical pharmacology, toxicology, regulatory , HEOR, market access, medical affairs ), applying foresight, scientific ... and will supervise and have accountability for the clinical components of regulatory filings. * Will contribute to overall Therapeutic Area disease strategy while… more
    Bristol Myers Squibb (12/03/25)
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