A global Regulatory Solutions organization is seeking a Regulatory Affairs Manager to support the development and execution of global regulatory strategies for investigational submissions, focusing on EU and UK Clinical Trial Regulations (CTR). The role involves managing lifecycle activities, ensuring compliance with regulatory requirements, and collaborating with a global team. Ideal candidates will have substantial experience in regulatory submissions and a strong attention to detail. Join the team to work on impactful initiatives supporting patient safety globally. #J-18808-Ljbffr