Associate Director Regulatory Affairs Europe
Acadia · Zug, Switzerland
7 YOE supervisor. Other duties as assigned. Education/Experience/Skills B.S. or M.S. with 7 years of relevant drug development experience , including 5 years relevant regulatory affairs experience in the EU. Ph.D., Pharm. D.,
This posting is pulled directly from Acadia's own Greenhouse page and applying happens on their site, not here. Posted 2026-09-03; Skip The Boards re-checks every company's board regularly and removes listings that disappear from the source.
More at Acadia
- Patient Access Manager Lead - Northeast
- Executive Neuroscience Sales Specialist - Austin, TX
- Senior Director, External Innovation
- Executive Assistant and Operations Manager
More jobs like this
- Principal Regulatory Affairs Specialist — Heartflow
- Director, Regulatory Affairs, Switzerland — Revolution Medicines
- AD/Director, Regulatory Affairs CMC — Bridgebio
- Regulatory Affairs Advisor — Natera
- Associate Director, Regulatory Affairs — Legend Biotech