EU CTR Submissions Lead | CTIS Expert & Regulatory Strategy

A mid-sized biotechnology company is seeking an EU CTR Submission Lead to manage regulatory submissions for clinical trials under EU Clinical Trial Regulation. This senior role requires 5+ years of experience in EU CTR submissions and strong communication skills. The successful candidate will ensure adherence to regulatory guidelines while leading cross-functional teams. Join us in delivering life-changing medicines and fostering innovation in our inclusive environment. #J-18808-Ljbffr