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
• Strong organizational and project management abilities
• Excellent analytical skills and attention to detail
• Strong communication and interpersonal skills
• Willingness to travel approximately 25%

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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