OverviewAs a Senior CRA, you oversee clinical trial monitoring to ensure adherence to protocol, GCP, and regulatory standards.
You operate within ICON's sponsor-dedicated model and collaborate with cross-functional teams to support trial execution.
You will train site staff, manage relationships with site personnel, and drive quality and continuous improvement.
This role offers integral exposure, a pathway for career development, and meaningful impact on patient outcomes.
Compensaciones / BeneficiosCompetitive base salary
Health and wellbeing programmes
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities
ResponsabilidadesMonitor sites to ensure compliance with study protocols, GCP, and regulatory requirements
Conduct site visits to assess performance, resolve issues, and support trial execution




Collaborate with cross-functional teams to ensure timely data collection and reporting
Provide training and guidance to site staff and fellow CRAs
Build and maintain relationships with site personnel and stakeholders to facilitate smooth operations
Requisitos principalesBachelor in relevant scientific discipline or healthcare-related field
Extensive experience as a Clinical Research Associate
Ability to manage multiple sites and projects simultaneously
Expertise in monitoring practices, data integrity, and site management
Proficiency in relevant clinical trial software and tools
Excellent communication and stakeholder management skills
Willingness to travel approximately 60%
communication
stakeholder management
problem-solving
monitoring practices
data integrity
site management

📌 Senior Clinical Research Associate (Barcelona)
🏢 Icon Clinical
📍 Barcelona