- Bristol Myers Squibb (Madison, NJ)
- …and/or review aggregate safety review documents as well as safety sections of relevant clinical trial documents and regulatory filings. . Lead team in the ... [DSUR], Periodic Benefit-Risk Evaluation Reports [PBRER]) and safety sections of relevant clinical trial documents (eg, protocols, clinical study reports… more
- Bristol Myers Squibb (Madison, NJ)
- …Team(s). + Oversee aggregate safety review documents and safety sections of relevant clinical trial documents and regulatory filings. + Coordinate evaluation & ... [DSUR], Periodic Benefit-Risk Evaluation Reports [PBRER]) and safety sections of relevant clinical trial documents (eg, protocols, clinical study reports… more
- AbbVie (Florham Park, NJ)
- …for bringing people, process, and technology together to generate business value from clinical trial . Our operational model is exemplified through execution and ... the strategy for Oncology in collaboration with CDSO Therapeutic head TA and will also support the growth and...to clinical data management. + Understanding of clinical trial methodologies, data collection processes, and… more
- Bristol Myers Squibb (Madison, NJ)
- …apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, ... in scale and scope, alongside high-achieving teams rich in diversity . Take your career farther than you thought possible....Director, US Medical Affairs (USMA) will report to the Head of USMA Cell Therapy and will be based… more
- Memorial Sloan-Kettering Cancer Center (New York, NY)
- …in pre- clinical development and IND application preparation for FDA-regulated clinical trial investigational products is required. Ph.D. in a scientific ... Kettering Institute, scientists across MSK collaborate to conduct innovative translational and clinical research that is driving a revolution in our understanding of… more