Senior Director, Clinical Affairs — FDA-Regulated Devices

Eight Sleep, Inc. is seeking a Director of Clinical Affairs to own end-to-end regulatory-driven clinical studies. This hands-on role requires building studies from scratch, managing sites, preparing IRB/ICFs, and overseeing data management and study committees to ensure on-time, on-budget execution.

You will bridge internal teams with investigators, CROs, IRBs, and regulatory agencies, bringing fluency in FDA device regulations and ICH-GCP to drive regulatory submissions and audits.