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 * Oversee safety reporting activities, management of protocol deviations, and ensure inspection readiness * Coordinate and collaborate with cross-functional teams, including Data Management, Clinical Research Associates (CRAs), and other relevant internal stakeholders * Provide regular written and verbal project updates to line management and ensure effective communication within the study team * Contribute to continuous process improvement initiatives, including SOP development and implementation of best practices in clinical operations * 7–10+ years of experience in clinical research, including clinical project management
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