Position Summary: The EU CTR Submission Lead is responsible for leading and overseeing the full lifecycle of regulatory submissions for clinical trials conducted under the EU Clinical Trial Regulation (EU CTR 536/2014) via the Clinical Trials Information System (CTIS). This role
Job Scope: What is this job’s focus? The Associate Director, EU CTR Strategy & Operations Excellence supports the Head of EU CTR in providing leadership and strategic oversight for the implementation, optimization, and continuous improvement of all EU Clinical Trials Regulation
Biogen is seeking an EU CTR Submission Lead based in Baar, Switzerland. This role is crucial for the successful oversight of regulatory submissions for clinical trials. The ideal candidate will manage the full lifecycle of submissions while ensuring
The Sr Director, Country & Site Operations (CSO), European Markets, is accountable for leadership and performance of country and site operations across assigned European markets, supporting Biogen clinical trials across all phases of development and therapeutic