Experteer Overview
As a Senior Clinical Research Associate at ICON, you will lead monitoring of clinical trials to ensure protocol compliance, regulatory adherence, and GCP standards. You’ll work across cross-functional teams to drive accurate data collection and issue resolution, while mentoring site staff to uphold high trial conduct standards. This role combines hands-on site monitoring with strategic collaboration to support efficient trial execution and quality improvement. You will travel approximately 60% to sites, shaping the conduct of multicenter studies within a mission-driven organization.

Compensaciones / Beneficios
• Monitor sites for protocol, regulatory, and GCP compliance
• Conduct site visits to assess performance and resolve issues
• Collaborate with cross-functional teams to ensure timely data collection and reporting
• Provide training and guidance to site staff and other CRAs




• Build and maintain relationships with site personnel and stakeholders to facilitate smooth operations

Responsabilidades
• Bachelor in a relevant scientific discipline or healthcare-related field
• Extensive experience as a Clinical Research Associate
• Ability to manage multiple sites and projects simultaneously
• Expertise in monitoring practices, data integrity, and site management
• Proficiency in relevant clinical trial software and tools
• Excellent communication, interpersonal, and stakeholder management skills
• Willingness to travel approximately 60%

Requisitos principales
• annual leave entitlements
• health insurance offerings
• retirement planning offerings
• LifeWorks Integral Employee Assistance Programme
• life assurance
• flexible country-specific optional benefits

📌 Senior CRA (Madrid)
🏢 Icon Clinical
📍 Madrid