• Senior Manager , CMC Global…

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …of regulatory guidelines and perspective to the cross-functional team. Serve as CMC regulatory lead on global project teams (Pharmaceutical Development, ... domestic/international travel. **Job Description** + Develop and implement global CMC regulatory strategies for late-stage development, marketing applications… more
    Otsuka America Pharmaceutical Inc. (12/02/25)
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  • Senior Manager , Global Regulatory…

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …of the associated regulatory challenges to the GRL, global regulatory team, assigned project teams, and internal/external functional business units ... associated regulatory challenges to the GRL, global regulatory team, assigned project teams, and internal/external...needed. - Works collaboratively with members of the global regulatory team (GRL, regional leads, CMC -RA, labeling,… more
    Otsuka America Pharmaceutical Inc. (11/20/25)
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  • Senior Manager , Global Product Quality…

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    … regulatory submissions for OPDC R&D products. Performs quality reviews of CMC sections of regulatory submissions. + Authors and maintains Standard Operating ... The Senior Manager , Global Product Quality - Biologics is responsible...Subsidiaries ensure Compliance with local and global requirements and regulatory requirements. + Interfaces with project teams… more
    Otsuka America Pharmaceutical Inc. (12/03/25)
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  • Sr. Non-Clinical Biostatistician

    Sanofi Group (Morristown, NJ)
    …Links with other internal and external stakeholders (such as R&D compliance, Functional Planner, Project Manager , CROs, etc.) + Under supervision of the senior ... diseases and bring hope to patients and their families. The Biostatistics Manager of the TED (Translational and Early Development) team supports Vaccine R&D… more
    Sanofi Group (12/17/25)
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  • Senior Vice President, Global Development…

    Bristol Myers Squibb (Madison, NJ)
    …program goals in compliance with GCP, ICH and other global regulatory requirements + Provides comprehensive strategic leadership for 2,100+ multi-site organization ... experience (20+years) of drug development or related experience managing clinical and CMC development under a variety of contexts; multiple clinical trials and… more
    Bristol Myers Squibb (12/05/25)
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