Senior Regulatory Publishing & eCTD Lead

A leading pharmaceutical company in St. Louis seeks a Senior Regulatory Publishing Specialist to coordinate the submission processes for regulatory compliance. Key responsibilities include managing eCTD submissions and ensuring compliance with FDA guidelines. The ideal candidate will have 5-7 years of experience in regulatory publishing, proficiency in electronic submission software, and a Bachelor's degree in a scientific discipline. Excellent communication skills and the ability to manage multiple projects are essential for success in this fast-paced environment. #J-18808-Ljbffr