Global Clinical Study Senior Manager

Role: Lead global clinical operations for one or more cancer-focused studies, ensuring end-to-end delivery from start-up to close-out. Responsibilities: oversee study planning, site activation, enrollment, data management, quality assurance, risk mitigation, and budget management; coordinate cross-functional teams including medical, regulatory, biometrics, and supply; serve as primary liaison to external partners and study teams; ensure regulatory compliance and inspection readiness; develop and optimize SOPs and work instructions. Requirements: Bachelor's in a scientific or healthcare discipline; 5+ years in clinical trial project management within biotech, pharma, or CRO sectors; proven experience leading clinical functions in oncology or related therapeutic areas; strong leadership, stakeholder management, and communication skills. Preferred: higher degree; experience with international oncology trials, GxP standards, and clinical systems (MS Office, project planning tools). High-value biopharma specifics: oncology focus, global scope, cross-regional study management, study start-up and enrollment expertise, regulatory compliance, and vendor oversight. Collaboration/reporting: interacts with BU Clinical Operations Lead, Biotech Unit Leadership, and cross-functional teams. Work setup: travel may be required; location modality not specified.