Experteer Overview

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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 xugodme
- 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 Global Employee Assistance Programme
- life assurance
- adaptable country-specific optional benefits

📌 Senior CRA (Madrid)
🏢 Icon Clinical
📍 Madrid