Global Regulatory Documentation Lead for Submissions

Bristol Myers Squibb in Warsaw seeks a Regulatory Document Author to lead the creation of various regulatory documents for product submissions. Candidates should have a PharmD or PhD, or relevant degree with five years of experience in regulatory documentation. Expertise in complex data analysis, strong writing skills, and familiarity with drug development processes are essential. The compensation range is between zł230,560 - zł279,377 for this full-time role, with additional incentive opportunities based on eligibility and experience. #J-18808-Ljbffr