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 / Beneficios Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Integral 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