Full-time

Manager, International Clinical Trial Regulatory Lead

Posted by Takeda • Zürich, Zurich, Switzerland

📍 Zürich, Zurich 🕒 March 01, 2026

Apply for this Job Similar Jobs

About the Role

Description  
Contributes to the development of regulatory strategy for assigned clinical trials in Europe & Canada (EUCAN) and Growth & Emerging Markets (GEM) regions. 
Develops the operational implementation plan for clinical trial applications (CTAs) in EUCAN and GEM regions from initial submission throughout lifecycle, in alignment with the global submission strategy. This may concern trials across a variety of Therapeutic Areas, including oncology, gastrointestinal and inflammation, marketed products and neuroscience. 
Executes or oversees all activities related to the creation, submission, management of Requests for Information (RFI) and maintenance of CTAs Globally (GEM and EUCAN region) in Europe through the EU Clinical Trial Information System (CTIS) or legacy processes in conformity with legal requirements and with Takeda’s global and regional internal procedures.  
Ensures oversight and tracking/or tracks CTA activities and e...
                

Job Details

Location Zürich, Zurich
Job Type Full-time
Category CAR
Posted March 01, 2026
Deadline April 10, 2026

Ready to Apply?

Submit your application today and take the next step in your career journey with Takeda.

Apply Now