Associate Director, Digital CMC & Regulatory Authoring

A global pharmaceutical company based in Washington, DC, is seeking an Associate Principal Scientist to optimize regulatory authoring processes. This role involves working on digital solutions for regulatory filings, aligning with business requirements, and developing data governance principles. A successful candidate will possess significant experience in the pharmaceutical industry, regulatory authoring, and data management initiatives. Collaboration with cross-functional teams is essential, alongside a strong focus on improving existing processes for product commercialization. #J-18808-Ljbffr