Develop, maintain, and track clinical project plans, timelines, budgets, and risk management strategies * 7–10+ years of experience in clinical research, including clinical project management * Minimum of 5 years of hands-on experience in clinical project management * Proven ability to manage multiple complex clinical projects simultaneously - 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 * Ensure all clinical studies are conducted in compliance with GCP (ISO 14155), EU MDR, and applicable local regulatory requirements * Coordinate and collaborate with cross-functional teams, including Data Management, Clinical Research Associates (CRAs), and other relevant internal stakeholders
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