EU CTR Submissions Group Lead – Regulatory Operations

A leading biotechnology company is looking for an EU CTR Submissions Group Lead to manage clinical trial submissions and lifecycle activities under EU regulations. This role includes overseeing a team of specialists, ensuring compliance with regulatory requirements, and leading operational excellence in submission processes. Ideal candidates have over 5 years of experience in EU clinical trials, strong leadership skills, and a background in pharma or biotech. Join us in delivering life-changing medicines. #J-18808-Ljbffr