Manage full-lifecycle implementation of Medable’s clinical trial software from kickoff through go-live and localization. Responsibilities include project planning, scope, budget, timelines, change management, risk mitigation, client communication, requirements translation, system enhancements, training, and cross-functional coordination. The role requires expertise in eCOA, ePRO, EDC, DCT, clinical trial data management, and regulatory compliance, while driving quality, process improvement, and successful client delivery.