Overview
Habilidades, experiencia, cualificaciones... Si tiene el perfil adecuado para esta oportunidad, asegúrese de inscribirse hoy mismo.

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 / Ventajas

- 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, regulatory, or clinical xqbhyrx 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
🏢 Jobrapido
📍 Barcelona