Experteer Overview
In this role you will foster strong relationships with clinical trial sites and guide them through study protocols and regulatory requirements. You’ll work cross-functionally to tailor site engagement strategies, monitor performance, and drive timely study conduct. You will contribute to ICON’s mission of advancing innovative therapies by enhancing site engagement and support. This is a chance to impact study success through collaborative, compliant, and proactive site partnerships.

Compensaciones / Beneficios
• Build and maintain relationships with key trial-site stakeholders (PI, site coordinators, research staff)
• Guide site staff on study protocols, procedures, and regulatory requirements to ensure compliance and successful conduct
• Identify opportunities to improve site engagement and performance via regular communication and feedback




• Collaborate with internal teams to develop and implement site engagement strategies tailored to each study/site
• Monitor site performance metrics and report engagement activities and outcomes to study teams

Responsabilidades
• Bachelor’s degree in life sciences or related field
• Experience in clinical research, site management, or related area
• Strong interpersonal and communication skills for diverse stakeholders
• Excellent organizational and problem-solving abilities with multitasking
• Knowledge of ICH-GCP guidelines and regulatory requirements
• Willingness to travel approximately 60%

Requisitos principales
• Competitive salary
• Annual leave entitlements
• Health insurance offerings
• Retirement planning offerings
• General Employee Assistance Programme LifeWorks
• Life assurance

📌 Site Engagement Liaison (Barcelona)
🏢 Icon Clinical
📍 Barcelona