Experteer OverviewAs a Senior Clinical Research Associate at ICON plc, you will oversee clinical trial activities to ensure compliance with protocols, regulatory requirements, and GCP.
You collaborate with cross-functional teams to secure data integrity and participant safety across the study lifecycle.
You will train site staff, support smooth trial execution, and nurture strong site relationships.
This role supports ICON's mission to advance clinical development through rigorous, ethical trials, offering meaningful impact and global travel opportunities.
Retribuzione / BenefitsMonitor trial sites for protocol adherence, regulatory compliance, and GCP
Conduct site visits to evaluate performance and resolve issues
Collaborate with cross-functional teams for timely data collection and reporting
Provide training and guidance to site staff and other CRAs
Build and maintain effective relationships with site personnel and stakeholders




ResponsabilitàAdvanced degree in a relevant field such as life sciences, nursing, or medicine
Extensive experience as a Clinical Research Associate
Proven ability to manage multiple sites and projects
Expertise in monitoring practices, data integrity, and site management
Proficiency in relevant clinical trial software and tools
Excellent communication, xysqume interpersonal, and stakeholder management skills
Ability to travel at least 60% and valid driver's license
Based in Rome, Venice and Florence area
Requisiti fondamentaliAnnual leave entitlements
Health insurance offerings
Competitive retirement planning
Global Employee Assistance Programme LifeWorks
Life assurance
Flexible country-specific benefits
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📌 Senior Clinical Research Associate (Lazio)
🏢 Experteer Italy
📍 Lazio