Associate Director, Digital CMC & Regulatory Authoring

A leading pharmaceutical company in Columbus, Ohio, is seeking an Associate Principal Scientist to enhance regulatory authoring processes. This position focuses on optimizing data management and digitizing the authoring of regulatory filings by collaborating with cross-functional teams. The ideal candidate will have significant experience in the pharmaceutical industry, project management skills, and a strong background in regulatory processes. This role offers a hybrid work model, ensuring a balance between in-office and remote work. #J-18808-Ljbffr