- Bristol Myers Squibb (Princeton, NJ)
- …and compiling technical documents that are critical for worldwide submissions. Senior Research Investigator , PBPK The scientist in this role will join ... as preclinical and clinical development. An individual is being sought at the Senior Research Investigator level and the site location is either Cambridge,… more
- Taiho Oncology (Princeton, NJ)
- …to transforming the landscape of cancer treatment and improving patients' lives. As a Senior Manager, Clinical Research Scientist , you will play a pivotal ... to be at the forefront of cancer research . Position Summary: The Senior Manager, Clinical Research Scientist has responsibility assisting in design,… more
- Bristol Myers Squibb (Princeton, NJ)
- …in their personal lives. Read more: careers.bms.com/working-with-us . Job Description The Senior Clinical Scientist reports through the Clinical Science function ... and CRA training materials and presentation at SIV and Investigator meetings and support on Study committee (eg, DMC)...+ 5+ years of experience in clinical science, clinical research , or equivalent + Proficient knowledge of GCP/ICH, drug… more
- Merck (Trenton, NJ)
- …Clinical Safety (GRACS) and external to GRACS. **Key functions:** + Reports to Senior Principal Scientist ( Senior Director) and/or Distinguished Scientist ... **Job Description** The Director/Principal Scientist , Regulatory Affairs Liaison, is responsible for the development and implementation of worldwide regulatory… more
- Sumitomo Pharma (Trenton, NJ)
- …. **Job Overview** We are currently seeking a versatile and experienced Senior Manager - Associate Director level scientist with strengths in ... diverse pipeline of early- to late-stage assets, we aim to accelerate discovery, research , and development to bring novel therapies to patients sooner. For more… more
- Taiho Oncology (Princeton, NJ)
- …related to the development program. + Perform data review supported by Clinical Research Scientist (s) (CRS), participate in protocol deviation meeting that will ... relevant clinical documents of high quality, such as study protocol protocol(s), investigator brochure (IB), informed consent forms (ICF), case report forms (CRF),… more