Overview

In this role you will oversee and drive the conduct of clinical trials to ensure alignment with protocol, GCP, and regulatory standards. You will monitor sites, manage data integrity, and support cross-functional teams to enable compliant, timely trial execution. You’ll train site staff, build strong relationships with stakeholders, and travel as needed to ensure successful study delivery. Join ICON’s inclusive, high-performing culture as you help shape the future of clinical development.

Compensaciones / Incentivos

- Various annual leave entitlements
- Health insurance offerings
- Competitive retirement planning
- General Employee Assistance Programme
- Life assurance
- Flexible country-specific optional benefits

Responsabilidades

- Monitor clinical trial sites for protocol, GCP, and regulatory adherence
- Conduct site visits to assess performance and resolve issues
- Collaborate with cross-functional teams to ensure accurate data collection and reporting




- Provide training and guidance to site staff and other CRAs
- Build and maintain relationships with site personnel and stakeholders for smooth operations

Requisitos principales

- Advanced degree in life sciences, nursing, or medicine
- Extensive experience as a Clinical Research Associate
- Ability to manage multiple sites and projects simultaneously
- Expertise in monitoring, data integrity, and site management
- Proficiency in relevant clinical trial software and tools
- Excellent communication, interpersonal, and stakeholder management skills
- Ability to travel at least 60% with a valid driver’s license

- Strong communication and interpersonal skills
- Stakeholder management
- Problem-solving and organizational skills
- Monitoring practices
- Data integrity
- Site management

📌 Sr. Clinical research Associate - barcelona
🏢 Icon Clinical
📍 Barcelona