Clinical Trial Manager

Role: Clinical Trial Manager within the Implantable Device Unit, supporting planning, coordination, and execution of clinical studies for Class III medical devices. Objectives include ensuring trial efficiency, regulatory compliance, data quality, and participant safety. Responsibilities involve monitoring trial progress, managing vendor and site relationships, tracking study activities, and resolving operational issues in collaboration with cross-functional teams such as Safety, Regulatory, and Quality. Requirements: Bachelor’s degree, minimum 5 years of experience in clinical research or operations, with specific experience supporting studies of Class III implantable devices, vendor/site management, and familiarity with regulatory protocols. Preferred: Advanced degree. High-Value: Focus on medical devices, clinical operations, vendor oversight, and site management; experience supporting complex regulatory environments; hybrid work location at Cambridge, MA, with no travel specified.