About the role

Ceribell in Sunnyvale, CA is seeking a Director of Clinical Affairs to define and execute the clinical evidence strategy for current and future products. You will lead trial design, coordinate with Regulatory Affairs, R&D, and Go-to-Market to align scientific plans with business goals. This role requires 8+ years in Clinical Research/Affairs in medical devices, strong GCP experience, and FDA/ISO knowledge. You will manage KOLs, oversee protocols, and shape regulatory submissions while building

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JOB OVERVIEW

Experience level

Manager

Location

Sunnyvale, CA

Occupation

Clinical Research Coordinators

Industry

Electromedical and Electrotherapeutic Apparatus Manufacturing

Posted

yesterday

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