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 / Ventajas * 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 o Competitive base salary o Performance-related incentives o Health and wellbeing programmes o Retirement and pension plans o Life assurance and disability coverage o Learning and development opportunities #J-18808-Ljbffr

📌 Global Country Operations Associate (España)
🏢 Icon Clinical
📍 España