Associate Director, Digital CMC & Regulatory Authoring

A leading pharmaceutical company in Hartford, Connecticut is seeking an Associate Principal Scientist to optimize regulatory authoring processes and enhance data management. The role involves defining project roadmaps, managing cross-functional teams, and setting data governance principles. Seeking candidates with extensive experience in regulatory authoring, project management, and data governance. This position supports a hybrid work model with flexible arrangements and requires a B.S. or higher in a relevant field, and a strong background in pharmaceuticals. #J-18808-Ljbffr