Descripción del trabajo
Experteer Overview As a SMA II at ICON, you support clinical trial site management and monitoring to ensure protocol adherence and GCP compliance. You work with cross-functional teams to facilitate site needs and deliver timely, accurate data and reports. The role contributes to accelerating patient access to new medicines by maintaining high-quality trial conduct. This is a values-driven, collaborative environment where you mentor junior staff and help scale how sites are managed across studies.
Compensaciones / Incentivos
Coordinate monitoring activities at clinical trial sites and resolve site-related issues promptly
Assist in preparing and reviewing regulatory documents to ensure GCP and regulatory compliance
Collaborate with cross-functional teams to support trial sites throughout the study lifecycle




Track site performance metrics, analyze data, and generate reports to improve site management efficiency
Participate in training initiatives and mentor junior staff in clinical trial management
Responsabilidades
Bachelor's degree in life sciences, healthcare administration, or clinical research
Experience in clinical research, site management, or monitoring with knowledge of GCP
Requisitos principales
Competitive base salary
Performance-related incentives
Health and wellbeing programmes
Retirement and pension plans
Life assurance and disability coverage
Learning and development opportunities
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📌 Global Country Operations Associate (Barcelona)
🏢 Icon Clinical
📍 Barcelona