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
- 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

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