Associate Director, Global Clinical Study Management

Role: Lead global clinical study management within biopharma, ensuring delivery aligns with timelines, budgets, and quality standards, particularly in oncology. Responsibilities: oversee all phases of complex studies, lead cross-functional teams including external vendors, manage study planning, execution, risk, quality, and regulatory readiness; develop SOPs and work instructions; ensure compliance with GxP, ICH/GCP, and inspection readiness; coordinate study budgets and resources; mentor junior members; collaborate with stakeholders and represent the study at leadership levels. Requirements: Bachelor’s in a scientific or healthcare field; 8+ years in clinical research, with proven experience managing global studies, preferably in oncology; strong leadership, project management, and operational expertise; advanced knowledge of clinical operations, tools (e.g., CTMS, project planning apps); ability to work independently on complex global projects. Preferred: higher degree and oncology-specific experience. High-Value: oncology, multiple phases including late-stage, global scope, cross-functional leadership, vendor management, GxP compliance, and risk mitigation. WorkSetup: travel may be required.