Experteer Overview In this role, you will oversee day-to-day clinical trial management to deliver high-quality outcomes across programmes. You will work with cross-functional teams to implement trial protocols, ensure regulatory and ethical compliance, and manage relationships with investigators and stakeholders. You will drive study deliverables, risk assessment, and vendor selection to maintain timelines and budgets. This position sits within ICON’s sponsor-dedicated model, contributing to treatments that benefit patients globally. You will collaborate in a collaborative, performance-driven environment that values inclusion and talent development.
Compensaciones / Incentivos
- Plan and manage all aspects of clinical trials to meet timelines, budget, and quality standards
- Collaborate with cross-functional teams to establish and implement trial protocols and procedures
- Build and manage relationships with trial investigators and stakeholders




- Ensure trials comply with local, national, and international regulations and ethical guidelines
- Problem-solve and make decisions on trial design, vendor selection, and risk managementResponsabilidades
- University degree in medicine, science, or equivalent combination of education u0026 experience
- Demonstrated ability to drive the clinical deliverables of a study
- Subject matter expertise in the designated therapeutic area
- Prior monitoring experience is preferred
- Willingness to travel approximately 25%Requisitos principales
- Various annual leave entitlements
- Health insurance offerings
- Competitive retirement planning
- Global Employee Assistance Programme LifeWorks
- Life assurance
- Flexible country-specific optional benefits

📌 Global Study Manager (Madrid)
🏢 Icon Clinical
📍 Madrid