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$200,000 – $250,000
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
This role leads the end-to-end design and execution of clinical studies for a medical device company, managing regulatory submissions, site coordination, and data operations. It suits someone with 10+ years of clinical ops experience who has successfully shepherded trials through FDA clearance and enjoys hands-on problem-solving in a fast-paced startup environment.
Our summary, not Eight Sleep’s wording. The full posting is on their site.
What they ask for
Required
- 10+ years of clinical operations for FDA-regulated medical devices or SaMD
- 5+ years in leadership roles executing clinical studies
- Experience managing third-party clinical sites
- Track record of authoring IRB submissions and informed consent forms
- 7+ years of cross-functional program management with clinical, engineering, and regulatory teams
- Strong knowledge of clinical data management and eCRF design
- Working fluency in FDA device regulations (IDE, De Novo, 510k), ICH-GCP, and ISO 14155
- Experience with study budgeting, vendor management, and CRO oversight
- Demonstrated participation in trials leading to FDA clearances or labeling expansions
- 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 work in high-growth startup or scale-up environments
- Experience supporting FDA breakthrough designations or pre-submission meetings