Experteer Overview In this role you will oversee clinical trial activities to ensure protocol alignment, regulatory compliance, and data integrity. You will monitor sites, conduct visits, and collaborate with cross-functional teams to support timely data collection and trial execution. You will train site staff, build strong relationships, and drive high standards of trial conduct. This position offers global exposure and a meaningful opportunity to shape the delivery of clinical development at ICON.
Retribuzione / Benefits Monitor trial sites for protocol adherence, regulatory requirements, and GCP standards
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 other CRAs to maintain high trial conduct standards
Cultivate relationships with site personnel and stakeholders to facilitate smooth trial operations




Responsabilità Advanced degree in life sciences, nursing, or medicine
Extensive experience as a Clinical Research Associate with strong regulatory knowledge
Proven ability to manage multiple sites and projects simultaneously with strong organizational skills
Expertise in monitoring practices, 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% of the time and possession of a valid driver's license
Requisiti fondamentali annual leave entitlements
health insurance offerings
retirement planning offerings
Global Employee Assistance Programme (TELUS Health)
life assurance
flexible country-specific optional benefits
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📌 Sr. Clinical Research Associate (Italia)
🏢 Altro
📍 Italia