Sr. Research Investigator/ Scientist - (New Brunswick, NJ)

The successful applicant will be part of the Analytical Regulated Testing GMP team at BMS New Brunswick New Jersey within Analytical Strategy & Operations. Assignments include conducting and overseeing cGMP analysis and analytical method validations. The responsibilities of a Project Coordinator (PC) provides strategy and oversight to analytical cGMP activities to support clinical and commercial development for small molecule New Chemical entities and Investigational Medicinal Products. Position duties include but limited to: - Effective collaboration and communication with the Integrated Development Team ensuring all API and drug product release testing, stability testing and filing requirements meet associated clinical timelines - Management of all analytical cGMP requirements from Phase I through Registrational filing to ensure project deliverable timelines are met.