ES
$140,000 – $175,000
Listed on Eight Sleep’s own careers site. You apply with them directly — we never stand between you and the employer.
What this role is
Eight Sleep seeks a hands-on Clinical Trial Manager to design, execute, and oversee medical device studies from protocol through submission, managing sites, data, and regulatory compliance. This role suits someone with deep FDA and clinical operations expertise who thrives in a startup environment and can build processes while delivering studies on time and budget.
Our summary, not Eight Sleep’s wording. The full posting is on their site.
What they ask for
Required
- 5+ years executing clinical studies for FDA-regulated medical devices or digital health products
- Hands-on experience managing third-party clinical sites including selection, activation, and monitoring
- Ability to author IRB submissions, informed consent forms, and clinical protocols
- 3+ years cross-functional program management with clinical, engineering, and regulatory teams
- Working knowledge of clinical data management and eCRF design
- Fluency in FDA device regulations (IDE, De Novo, 510(k) requirements) and ICH-GCP
- Experience with clinical study budgeting and CRO oversight
- Bachelor's degree
Nice to have
- Advanced degree (MS, MPH, PhD, or clinical doctorate)
- ACRP or SOCRA certification
- Experience with biosensing or consumer health devices
- Familiarity with real-world evidence study designs or decentralized trials
- Prior startup experience building processes from scratch
- Experience supporting FDA breakthrough device designations or pre-submission meetings