OverviewIn this role you oversee clinical trial monitoring to ensure adherence to protocol, regulatory standards and GCP, driving quality and continuous improvement.
You will lead site visits, collaborate with cross-functional teams and mentor site staff, ensuring smooth trial execution.
Your work supports ICON's mission to bring new medicines to patients faster by maintaining rigorous data integrity and site performance.
You will engage with site personnel and stakeholders, influencing compliance and operational excellence.
This is a globally-facing role with significant travel and impact across multiple trials.
Retribuzione / BenefitsCompetitive base salary and performance-related incentives
Health and wellbeing programmes (medical, dental, vision)
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities and structured career pathways
ResponsabilitàMonitor trial sites for protocol compliance, regulatory adherence, and GCP standards
Conduct site visits to assess performance, resolve issues, and support successful execution




Collaborate with cross-functional teams to ensure timely, accurate data collection and reporting
Provide training and guidance to site staff and other CRAs to maintain high trial conduct standards
Build and maintain effective relationships with site personnel and stakeholders to facilitate operations
Requisiti fondamentaliBachelor in relevant scientific discipline or healthcare-related field
Extensive experience as a Clinical Research Associate with strong understanding of trial processes and regulatory requirements
Proven ability to manage multiple sites and projects simultaneously with strong organizational and problem-solving skills
Expertise in monitoring practices, data integrity, and site management; proficient in relevant clinical trial software and tools
Excellent communication, interpersonal and stakeholder management skills; ability to influence and drive compliance in a complex environment
Willingness to travel approximately 60%
strong communication
interpersonal skills
stakeholder management
monitoring practices
data integrity
site management

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