Descripción del trabajo
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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

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- 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

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- Bachelor's degree in life sciences, healthcare administration, or clinical research

- Experience xhfqzwm in clinical research, site management, or monitoring with knowledge of GCP
Requisitos principales

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- 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