Global Regulatory Submissions Lead – RD&E & Delivery

A leading pharmaceutical company is seeking a Global Regulatory Associate to manage registration processes in Indianapolis, Indiana. This role involves ensuring compliance with submission regulations and collaborating with cross-functional teams. The ideal candidate will have a BS in a technical or scientific discipline and at least 2 years of experience in the drug development process. Strong project management and organizational skills, along with the ability to influence and negotiate, are essential for success in this position. #J-18808-Ljbffr