Experteer Overview

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In this role you drive delivery quality for Phase I–IV studies, Epidemiology, and Real World Evidence across sponsor programs. You lead CSL/CRM activities, oversee risk-based site management, and ensure timely, cost-efficient execution in a global, sponsor-dedicated model. You partner with internal and external teams to implement operational excellence and data-driven planning, shaping study delivery at scale. The position sits in ICON’s Functional Service Provision division, enabling collaboration with CROs and pharma partners.

Compensaciones / Beneficios
• Provide leadership and strategic direction for CSLs/CRMs across assigned programs
• Drive delivery accountability among internal/external partners for study execution
• Implement operational excellence strategies and data-driven planning
• Identify and mitigate risks affecting timelines, quality, and costs
• Establish risk-based site oversight and monitoring plans




• Escalate trends and issues to leadership with actionable mitigation
• Onboard and upskill ICSO team members; promote knowledge sharing
• Link CSLs/CRMs with General functions as single point of contact for operations
• Lead regular CSL/CRM calls and participate in Investigator/Study Coordinator Meetings
• Oversee Company Sponsored, Collaborative Research, and Investigator Sponsored Studies across portfolio
• Act as global operations lead for Early Access activities with Medical Affairs
• Review governance compliance and contribute to feasibility guidance
• Monitor program-level dashboards to manage risk and finance impact
• Collaborate with GMA and Launch/Brand teams for information sharing
• Represent CTE at governance boards and provide guidance on site feasibility
• Design country start-up strategies with Start-up Solutions Team and CSS
• Develop site oversight plans and data-driven oversight tools
• Identify opportunities

📌 Trial Clinical Delivery Lead (Madrid)
🏢 Icon Clinical
📍 Madrid