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 operationsResponsabilidades
- 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 General Employee Assistance Programme
- life assurance
- flexible country-specific optional benefits

📌 Senior Cra (Madrid)
🏢 Icon Clinical
📍 Madrid