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 PDC
What its about Join Partners Group’sClient Content Evergreensteam at the center of our Evergreens fundraising momentum – shaping the product story and bringing investment insights to life through best-in-class client materials. In this role, you will
About This Role: As the International Commercial Lead for Alzheimer’s Disease, you will drive performance, strategic direction, and commercialization excellence across diverse international markets. This pivotal role involves ensuring strong alliance governance, effective cross-regional alignment, and
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 The Senior Director, Alzheimer’s Global Diagnostics & Disease Area Strategy, will lead the overall global AD diagnostic pathway strategy and disease area strategy for the Alzheimer’s Disease and Dementia Franchise. Significant collaboration is
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
About This Role: The Global Launch and Commercial Operations Lead is a senior individual contributor accountable for the end‑to‑end governance, readiness, and execution excellence of Biogen’s global commercial launch of zorevunersen — a potential first-in-class disease-modifying
About This Role The Senior Medical Director, Global Medical Affairs, Nephrology will be a strategic partner providing expert medical leadership to guide medical strategy development, launch planning, and support for our Glomerular Nephritis programs, including IgAN and
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