Global Regulatory Medical Writing Program Lead

A leading biotech firm in North Carolina is seeking an experienced Program Manager for its Regulatory Medical Writing team. This role involves leading high-visibility client programs, managing relationships, and ensuring the quality and timeliness of multiple documents. Candidates should have a Bachelor’s degree in a scientific discipline, at least 8 years of relevant experience, and strong program management skills. The position offers the chance to work in a collaborative, innovative environment that values scientific excellence. #J-18808-Ljbffr