- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …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
- Bristol Myers Squibb (Cambridge, MA)
- …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 (Cambridge, MA)
- …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