• Senior Manager , Global…

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …pharmaceutical and/or healthcare industry. - Knowledge and experience with preparation of global regulatory submissions (IND, CTA , NDA or BLA, MAA). - RAC ... **Position Summary** Provides critical support in developing global regulatory strategy, planning and execution of global investigational and marketed prescription… more
    Otsuka America Pharmaceutical Inc. (11/20/25)
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  • Senior Director, Program Management,…

    Bristol Myers Squibb (Princeton, NJ)
    …experience in all phases of research and drug development, including global regulatory submissions (IND/ CTA through NDA/BLA/MAA/JNDA/ NDA China) and lifecycle ... personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Senior Director, Program Management Lead (individual contributor) is assigned… more
    Bristol Myers Squibb (11/22/25)
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  • Director, Program Management

    Bristol Myers Squibb (Princeton, NJ)
    …in nearly all phases of research and drug development, including global regulatory submissions (IND/ CTA through NDA/BLA/MAA/JNDA/ NDA China) and lifecycle ... planning including annual and long-term portfolio processes. + May serve as a matrix manager for Program Management resources assigned to the asset. + Supports DD PM… more
    Bristol Myers Squibb (11/25/25)
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