Senior Clinical Study Manager (Hybrid) at Stryker

The Senior Clinical Study Manager will be responsible for the day-to-day management of one or more clinical studies, including IDE, post-approval, post-market surveillance, feasibility, marketing, and investigator-initiated studies. This role involves leading the development of project charters and management plans, owning the project schedule through Gantt charts, defining and managing project scope with Work Breakdown Structures, and developing and maintaining project budgets. The manager will also create and monitor project Quality Plans, identify and manage project risks with response plans, establish procurement strategies, and assign and manage cross-functional resources.