You will act as a trusted quality and compliance advisor. You will help teams navigate complex regulatory requirements, strengthen quality processes, manage risk and continuously improve the way clinical trials are delivered. Monitor the regulatory
Act as a Program Lead to provide oversight of a program within the organization providing oversight to a group of studies and Data Management Leads ensuring that the studies within the program are delivered per corporate goals and objectives.
Develop bioanalytical (especially LC/MS/MS) methods for the discovery and development of NCEs (New Chemical Entities) or NBEs (New Biological Entities). Operate and maintain LC-MS/MS instrumentation, ensuring proper calibration, troubleshooting, and
You'll be a recognised expert and a key contributor to the strategic direction of Risk-Based Management across the company; including representing BMS externally with industry groups and key partners. You'll work with a significant portion of BMS's