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 regulatory and quality functions for medical device products: shape risk management, oversee the QMS, manage regulatory submissions (FDA 510(k)/De Novo), ensure standards compliance (ISO 13485/14971), and implement post-market monitoring while coordinating with R&D, Clinical, and Operations.

The Growth Marketing Manager will lead digital advertising campaigns, optimize marketing performance through data analysis, and implement automation tools, while collaborating across teams to drive growth.