Experteer Overview

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In this role you will oversee global study delivery from CSP development through study close-out, coordinating with internal teams and external vendors to ensure on-time, on-budget, and high-quality (CSR-related) deliverables. You will align with the Study Lead and drive vendor scope, oversight, and performance metrics across multiple therapeutic areas. You will manage start-up, recruitment, and site activities, contribute to study documents, and support continuous improvement through lessons learned. This position offers the opportunity to shape global study execution within a collaborative Development Operations environment.

Compensaciones / Ventajas
• Strategize and oversee key vendors to meet timelines, budget, and quality; maintain oversight documentation across the study life cycle
• Coordinate cross-functional activities including Data Management, Regulatory, Patient Safety, QA,



and CROs to enable efficient study delivery
• Plan and conduct internal/external meetings (e.g., Investigators'/Monitors' meetings)
• Support budget management and external service provider invoicing; assist with study documents/plans
• Perform Study Lead activities for less-complex studies and delegate team responsibilities
• Lead lessons learned exercises and contribute to departmental initiatives and SME functions
• Coordinate start-up and recruitment activities across countries and monitor sites globally
• Oversee country activities during protocol amendments, database locks, and Investigator Meetings; manage site close-out and post-trial activities
• Provide study-related training and support country teams with resourcing and CRA development
• Develop/review study documents including training materials and monitoring/oversight plans
• Aggregate and communicate deliverables to the CTT and country xghoner teams
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📌 Global Study Manager (Barcelona)
🏢 Alexion Pharmaceuticals
📍 Barcelona