• Senior Director, Innovative Statistics

    Cytel (Trenton, NJ)
    …unique knowledge in related areas (adaptive designs, clinical development, data science , model-informed drug development), to provide strategic advice to define ... optimal regulatory , clinical and/or market access pathways and promote faster...in Mathematics, Biostatistics, or a related field; MBA, MD, PhD or advanced degree highly desirable; at least 15+… more
    Cytel (08/12/25)
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  • Sr Staff Scientist - Medical Device

    Astrix Technology (Essex County, NJ)
    **Sr Staff Scientist - Medical Device** Science & Research Essex County, NJ, US Pay Rate Low: 128000 | Pay Rate High: 184000 + Added - 27/05/2025 Apply for Job _Our ... initiatives across product development, method validation, risk assessment, and regulatory compliance. **Key Responsibilities:** + Lead the design and execution… more
    Astrix Technology (08/11/25)
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  • Technical Fellow (Director), Advanced Therapies…

    J&J Family of Companies (Raritan, NJ)
    regulatory inspections, and health authority questions. **Qualifications:** + PhD in Chemical Engineering, Microbiology, Cell Biology, or related with 10-12 ... Innovative Medicine is informed and inspired by patients, whose insights fuel our science -based advancements. Visionaries like you work on teams that save lives by… more
    J&J Family of Companies (08/09/25)
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  • Medical Director, Clinical Research

    J&J Family of Companies (Raritan, NJ)
    …Innovative Medicine is informed and inspired by patients, whose insights fuel our science -based advancements. Visionaries like you work on teams that save lives by ... the Compound Development Team (CDTL) and project management, global regulatory affairs, clinical pharmacology, health economics, and the disease...- External** + An MD is required; Advanced degree ( PhD ) is a plus. + A minimum of 2… more
    J&J Family of Companies (08/01/25)
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  • Associate Director, MSAT, Upstream

    Otsuka America Pharmaceutical Inc. (Princeton, NJ)
    …professional to join our organization as the Assoc. Director of Manufacturing Science and Technology (MSAT) for Upstream processes. This critical role will lead ... and/or review technical reports, protocols, risk assessments, and relevant sections of regulatory submissions (IND, BLA, MAA, etc.) related to upstream processing. +… more
    Otsuka America Pharmaceutical Inc. (07/18/25)
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  • Medical Director, Global Medical Affairs, Early…

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …public groups, government officials, medical societies) about Our Company's emerging science . + Ensure peer relations within Otsuka across functions at appropriate ... and strong competency with the US healthcare system and regulatory landscape is required for this role. + Stay...leadership meetings and plans. **Requirements:** + Medical Doctor (MD), PhD or PharmD candidates with demonstrated experience in CNS… more
    Otsuka America Pharmaceutical Inc. (07/16/25)
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  • Remedial Investigations Discipline Leader

    CDM Smith (Elizabeth, NJ)
    …Licensed Professional Geologist or professional scientist registration/certification * Master's degree or PhD in science or related discipline. * Knowledge and ... is required. Expertise in PFAS characterization, familiarity with evolving regulatory frameworks, and challenges with emerging contaminants is desired. Understanding… more
    CDM Smith (07/29/25)
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  • Principal Scientist Transporters

    Bristol Myers Squibb (Princeton, NJ)
    …critical experiments. Effectively communicate findings to teams, prepare and review regulatory source reports. + Troubleshoot and optimize in vitro transporter ... + Contribute to the strategic direction of the Transporter Group, expanding our science and staying current with literature. Publish and present at internal and… more
    Bristol Myers Squibb (07/29/25)
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  • Director, Integrated Publications

    Taiho Oncology (Princeton, NJ)
    …collaborators and partners, and each other. Together, we are working on cutting-edge science and growing our portfolio and pipeline across a range of tumor types ... plan for scientific and clinical studies in process, prior to regulatory submissions, and assessment of secondary publication plan development and alignment… more
    Taiho Oncology (07/25/25)
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  • Associate Director, Business Development, Search…

    Bristol Myers Squibb (Princeton, NJ)
    …core leadership qualities. A deep understanding of drug discovery, development, and regulatory processes is required, as the candidate will lead both scouting ... such as presentations, FAQ and related documents. **Qualifications & Experience** + MD, PhD , PharmD, or other advanced degree in the biomedical field required +… more
    Bristol Myers Squibb (08/13/25)
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