Senior Global Clinical Study Manager

Senior Global Clinical Study Manager responsible for end-to-end planning and execution of clinical trials across multiple regions. Oversees site management, enrollment, monitoring, and closeout while managing stakeholder relationships, budgets, and regulatory compliance.

Responsibilities

• Lead site selection, activation, recruitment performance, and monitoring strategy throughout study lifecycle
• Serve as primary client contact and manage cross-functional teams across regions and cultures
• Develop integrated study plans, identify risks, and implement mitigation and corrective actions
• Manage study budgets, forecasting, billing reviews, and financial performance tracking
• Ensure compliance with GCP standards, protocols, regulatory requirements, and trial management file health

Requirements

• Bachelor's degree in life sciences or related field
• 5+ years clinical research/monitoring experience with 2+ years in study management
• 2+ years global study management across multiple countries and regions
• Phase I–III clinical trial experience with Phase III required
• Oncology experience required
• Strong ICH-GCP and FDA regulatory knowledge
• Demonstrated project financial management and Microsoft Office proficiency

Compensation: $93,100–$232,800 base