Regional Clinical Study Manager

Role: Lead regional clinical operations for cancer-focused studies, overseeing study delivery, vendor management, and compliance. Responsibilities: manage regional study timelines from feasibility to closeout, ensure inspection readiness, oversee external vendors and internal teams, coordinate with stakeholders, and maintain study quality and regulatory compliance. Manage budgets, resources, and site selection, and support data collection and reporting activities. Requirements: Bachelor's degree in a scientific or healthcare discipline (advanced degree preferred), 4+ years of experience in clinical research within biotech, pharma, or CRO, with proven leadership and possibly CRA background. HighValue: Oncology, cancer indications, clinical stage (pre- or active trials), study management, vendor oversight, regulatory compliance, GxP. WorkSetup: travel may be required; location flexible based on business needs.