- Bristol Myers Squibb (Princeton, NJ)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Senior Principal Scientist role will be responsible for development ... programs. Key responsibilities of this role are to act as a lead scientist to deliver and implement biomarker strategies for clinical programs, develop reports… more
- Bristol Myers Squibb (Princeton, NJ)
- …+ Develops and executes translational disease strategy in the pancreatic cancer (PC) area with deep disease expertise + Leads and oversees execution of disease ... strategy including but not limited to various aspects of patient selection strategies + Serves as scientific expert in generating novel hypotheses for actionable biology based on novel discoveries integrating disease work with literature and deep expertise in… more
- Merck (Trenton, NJ)
- …and Clinical Safety (GRACS) and external to GRACS. **Key functions:** + Reports to Senior Principal Scientist ( Senior Director) and/or Distinguished ... **Job Description** The Director/ Principal Scientist , Regulatory Affairs Liaison, is...and associated documentation. Provide expertise as the Global Regulatory Lead to Product Development Teams and the regulatory single… more
- RELX INC (Trenton, NJ)
- Principal Data Scientist I Are you looking to...for our customers and communities. About the Role: As a Senior Data Scientist , you will become a subject ... model development Requirements: + Have substantial experience in a senior data scientist role + Have experience...Be a natural problem solver, able to take a lead in collaborating to resolve issues + Have excellent… more
- Bristol Myers Squibb (Princeton, NJ)
- …acting on clinical trial data to support development + Serving as principal functional author for Regulatory submission, study reports, and publications + Provides ... lifecycle + Manages site interactions in partnership with the Clinical Scientist for medical questions and education (including safety management guidelines) +… more
- Bristol Myers Squibb (Princeton, NJ)
- …on Clinical Trial data to support development, and + Serving as principal functional author for Regulatory submission, study reports, and publications + Provides ... lifecycle + Manages site interactions in partnership with the Clinical Scientist (CS) for medical questions and education (including safety management guidelines)… more