Overview
La siguiente información ofrece un resumen de las habilidades, cualidades y cualificaciones necesarias para este puesto.
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 general health research context.
Compensaciones / Beneficios
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 discipline or equivalent clinical research experience
Experience in site support, site activation, start-up, xqbhyrx regulatory, or clinical trial operations in CRO/pharma or similar environment
Hands-on experience with EU CTR processes
Good understanding of clinical trial documentation, GCP and site-level regulatory requirements
Fluent in Spanish and English with strong communication skills
Strong organizational skills with ability to manage multiple sites and deadlines
Proactive, solution-focused approach and confident working with investigator sites and cross-functional teams
proactive problem-solving
strong communication
organization and time management
EU CTR processes
GCP and site regulatory requirements
clinical trial documentation

📌 Site Specialist II (Barcelona)
🏢 Icon Clinical
📍 Barcelona