Responsibilities: Design and manage clinical studies to validate company products and services. Develop study documents (Protocols, Data Management Plan, Statistical Analysis Plan, etc.) and coordinate with clinical trials partners for site communication. Work with clinical data to monitor quality and escalate technical issues. Oversee clinical research projects, ensuring timely delivery of milestones and coordination of study execution. Manage regulatory documentation for audit readiness. Visit clinical sites in Europe and the US for study setup, monitoring, and compliance with regulations and guidelines. Report progress to the clinical and algorithm teams, as well as executive management. Develop and maintain study materials in compliance with regulations. Provide guidance on best practices for clinical study design and execution.