Experteer Overview
As a Clinical Research Associate I at ICON Strategic Solutions, you contribute to clinical trial operations within a sponsor-dedicated model, collaborating across teams to deliver high-quality monitoring outcomes. You will coordinate setup and monitoring activities, generate study status reports, and maintain documentation while ensuring patient safety and regulatory compliance. The role involves sponsor-driven queries, cost efficiency, and preparation of study materials, with substantial travel to sites. You join a diverse, supportive culture focused on patient impact and professional development.

Compensaciones / Beneficios
• Coordinate setup and monitoring activities for a study and maintain study documentation
• Complete accurate study status reports and manage sponsor-generated queries
• Participate in feasibility studies and review of study documentation for new proposals
• Develop strong collaboration with stakeholders,



investigators, and site staff
• Ensure patient safety through compliance with procedures, protocols, and regulatory requirements

Responsabilidades
• University degree in medicine, science, or equivalent
• Knowledge of ICH-GCP guidelines and ability to review/interpret medical data
• Excellent written and verbal English communication
• Strong interpersonal skills to handle queries promptly
• Willingness to travel approximately 60%
• Relevant clinical trial monitoring experience

Requisitos principales
• Annual leave entitlements
• Health insurance offerings
• Competitive retirement planning
• Integral Employee Assistance Programme LifeWorks
• Life assurance
• Flexible country-specific optional benefits

📌 Clinical Research Associate 1 (Barcelona)
🏢 Icon Clinical
📍 Barcelona