Eight Sleep Benefits Overview

Lead end-to-end execution of regulatory-driven clinical studies for FDA-regulated devices and SaMD. Design protocols, manage IRB/ICF submissions, oversee site selection/monitoring and CROs, ensure data quality and regulatory compliance, support FDA submissions and audits, and build scalable clinical operations, timelines, budgets, SOPs, and cross-functional alignment to deliver studies on time and on budget.

Lead full-cycle recruiting for a portfolio of global roles: proactively source, engage, and close top talent; partner with hiring managers; maintain ATS workflows and dashboards; optimize processes to reduce time-to-fill while preserving a high talent bar and strong culture fit.

Build and ship marketing and campaign landing pages using React/Next.js; design and run A/B experiments end-to-end; maintain analytics and tracking (Amplitude, GTM, GA4); optimize conversion, SEO, accessibility, performance, and localization; create templatized systems for rapid launches and ensure privacy-compliant event data.