Overview

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As Site Specialist II at ICON, you support clinical trial sites in Spain to drive start-up, activation, and ongoing site management. You act as a key operational contact for Spanish investigator sites and internal study teams, ensuring regulatory activities, documentation, and milestones are managed accurately. The role requires hands-on EU CTR knowledge and collaboration across regulatory, clinical operations, and site teams. You will identify delays, drive follow-ups, and contribute to process improvements that accelerate study timelines. This position offers meaningful work shaping site operations in a global health research context.

Compensaciones / Incentivos
- Competitive base salary and performance related incentives
- Health and wellbeing programmes
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities





Responsabilidades
- Coordinate collection and maintenance of essential site documentation to ensure regulatory compliance
- Support site start-up and regulatory activities per EU CTR requirements
- Act as operational contact for Spanish investigator sites, guiding documentation, systems, timelines, and processes
- Track site progress, milestones, and actions within clinical trial management systems
- Collaborate with Site Activation, Regulatory, Clinical Operations and cross-functional teams to resolve issues impacting timelines
- Support ongoing site maintenance throughout the study lifecycle
- Proactively identify delays or operational challenges and drive follow-up with sites and stakeholders
- Contribute to process improvements and share best practices
- Provide guidance and support to junior colleagues as appropriate

Requisitos principales
- Bachelor’s degree in life sciences, healthcare or related

📌 Site Specialist II (Barcelona)
🏢 Jobrapido
📍 Barcelona