- Merck (Trenton, NJ)
- …**Role Summary:** + The Global Director Medical Affairs (GDMA) is responsible for supporting the execution of scientific & medical affairs plans for their assigned ... Therapy Areas (TA) in key countries and regions. They are impactful members of Product Development Team sub-teams and Global Human Health commercialization teams. They collaborate with Early and Late Development Company Research Laboratories functional areas,… more
- 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 and… more
- Bristol Myers Squibb (Princeton, NJ)
- …track record of high-quality scientific publications in relevant fields For the Sr. Principal Scientist position, the starting compensation for this job is a ... human genetics, immunology). + Minimum of 6 years post-PhD experience for Sr. Principal Level (and minimum of 8 years Post-PhD experience for AD Level), with… 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
- 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 ... for model development Requirements: + Have substantial experience in a senior data scientist role + Have experience in leading complex projects and customer… 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