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
About This Role This person is a hands-on leader with responsibility for advancing the execution of significant elements of program strategy and cross-functional execution for the Dravet (Zorevunersen) program. Strong performance in this role enables the Zorevunersen
This is what you will do: The Alpine (Switzerland & Austria) Team Coordinator will support the General Manager CENE and the cross-functional teams (commercial, Medical, Access,…) by providing a broad administrative and operational support including general administration,
This is what you will do: The Alpine (Switzerland & Austria) Team Coordinator will support the General Manager CENE and the cross-functional teams (commercial, Medical, Access,…) by providing a broad administrative and operational support including general administration,
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