Regional Clinical Study Manager

Role: Regional Clinical Operations Lead responsible for study delivery, inspection readiness, and team management within a specified region for oncology or cancer-related trials. Objectives include ensuring timely, compliant trial execution, managing external vendors, and maintaining study quality. Responsibilities encompass leading regional teams, overseeing planning from feasibility to closeout, coordinating with cross-functional stakeholders, and managing budgets and resources. The role involves ensuring regulatory compliance, preparing for audits and inspections, and driving data quality and study documentation. Qualifications: Bachelor's degree in a scientific or healthcare field (higher degree preferred), 6+ years of progressive clinical research experience in biotech, pharma, or CRO, with demonstrated leadership in clinical operations; CRA experience preferred. Skills include proficiency in MS Office and project planning tools. High-value specifics: focus on cancer indications, regional study management, inspection readiness, and cross-functional collaboration; travel may be required. The role reports to senior management and involves supervising team members and external vendors.