- Ascendis Pharma (Princeton, NJ)
- …We offer a dynamic workplace for employees to grow and develop their skills. The Regulatory Project Manager will be an integral part of Global Regulatory ... Affairs, providing project management leadership to key global regulatory submissions across the Ascendis pipeline. As a part of the Global Regulatory Affairs… more
- 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
- Sanofi Group (Morristown, NJ)
- **Job Title:** Senior Clinical Research Director **Location:** Cambridge, MA or Morristown, NJ **About the Job** Join the engine of Sanofi's mission - where deep ... breakthroughs that could turn the impossible into possible for millions. As the ** Senior Clinical Research Director** ( Senior CRD) within the RARE Therapeutic… more
- 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 (Princeton, NJ)
- …team supporting workstreams of a large, highly complex late stage GPTs with oversight of a Senior PM. As a Program Manager , this team member is assigned at the ... Program Management (PM) will be assigned as a Program Manager and work under the matrix leadership of a...varied experience in research and drug development, including global regulatory submissions (IND/ CTA through NDA/BLA/MAA/JNDA/ NDA China)… more