Description
Bristol Myers Squibb is hiring a Scientific Writer II (Manager level) to lead document strategy and author regulatory documents supporting submissions and approvals across key markets and geographies. The role coordinates and writes fit-for-purpose regulatory documents such as Investigator’s Brochures, safety reports, clinical study reports, and protocols, integrating scientific, medical, and regulatory input from cross-functional teams while managing timelines, quality, review cycles, and document tools/processes. The position is site-design/hybrid.
