- Merck (Trenton, NJ)
- **Job Description** The Director / Principal Scientist , Regulatory Affairs Liaison, is responsible for the development and implementation of worldwide ... regulatory strategy for their assigned projects in the General...external to GRACS. **Key functions:** + Reports to Senior Principal Scientist (Senior Director ) and/or… more
- Merck (West Point, PA)
- **Job Description** Under the general direction of a Senior Director , Epidemiology, the Principal Scientist , Epidemiology, has responsibility for the design, ... with risk management sub-teams, Value and Implementation (V&I) sub-teams, clinical, and regulatory sub-teams, and other R&D areas on epidemiologic matters related to… more
- Bristol Myers Squibb (Princeton, NJ)
- …acting on Clinical Trial data to support development, and + Serving as principal functional author for Regulatory submission, study reports, and publications + ... at work and in their personal lives. Read more: careers.bms.com/working-with-us . ** Director , Early Clinical Development (MD) - Hematology & Cell Therapy with Focus… more
- Bristol Myers Squibb (Princeton, NJ)
- …and acting on clinical trial data to support development + Serving as principal functional author for Regulatory submission, study reports, and publications + ... their personal lives. Read more: careers.bms.com/working-with-us . **Job Title** Director , Early Clinical Development - Immunology **Functional Area Description**… more
- Merck (North Wales, PA)
- …Summary** + Under the guidance of a senior leader, an Associate Principal Scientist /Associate Director , has primary responsibility for planning/managing ... barriers to reimbursement and market access, and provide input into clinical, regulatory , payer/access, marketing and evidence generation strategy and programs + In… more