Overview
¿Está pensando en solicitar este empleo? No se demore, desplácese hacia abajo y envíe su solicitud lo antes posible para no perder la oportunidad.
In this role you will oversee and drive the conduct of clinical trials to ensure alignment with protocol, GCP, and regulatory standards. You will monitor sites, manage data integrity, and support cross-functional teams to enable compliant, timely trial execution. You’ll train site staff, build strong relationships with stakeholders, and travel as needed to ensure successful study delivery. Join ICON’s inclusive, high-performing culture as you help shape the future of clinical development.
Compensaciones / Beneficios
Various annual leave entitlements
Health insurance offerings
Competitive retirement planning
Integral Employee Assistance Programme
Life assurance
Flexible country-specific optional benefits
Responsabilidades
Monitor clinical trial sites for protocol, GCP, and regulatory adherence
Conduct site visits to assess performance and resolve issues




Collaborate with cross-functional teams to ensure accurate data collection and reporting
Provide training and guidance to site staff and other CRAs
Build and maintain relationships with site personnel and stakeholders for smooth operations
Requisitos principales
Advanced degree in life sciences, nursing, or medicine
Extensive experience as a Clinical Research Associate
Ability to manage multiple sites and projects simultaneously xqbhyrx
Expertise in monitoring, data integrity, and site management
Proficiency in relevant clinical trial software and tools
Excellent communication, interpersonal, and stakeholder management skills
Ability to travel at least 60% with a valid driver’s license
Strong communication and interpersonal skills
Stakeholder management
Problem-solving and organizational skills
Monitoring practices
Data integrity
Site management

📌 Sr. Clinical research Associate (Barcelona)
🏢 Icon Clinical
📍 Barcelona