Coordinate and collaborate with cross-functional teams, including Data Management, Clinical Research Associates (CRAs), and other relevant internal stakeholders - To enlarge our Clinical Programs EMEA team we are looking as soon as possible for a * Lead the end-to-end management of clinical studies for Class III medical devices, from feasibility assessment through study close-out * Develop, maintain, and track clinical project plans, timelines, budgets, and risk management strategies * Ensure all clinical studies are conducted in compliance with GCP (ISO 14155), EU MDR, and applicable local regulatory requirements * Monitor overall study progress, patient enrollment, data quality, and achievement of key milestones * Contribute to continuous process improvement initiatives, including SOP development and implementation of best practices in clinical operations
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