As a Senior Clinical Research Associate at ICON, you will lead clinical trial monitoring to ensure adherence to protocols, regulatory requirements, and GCP standards. You will monitor sites, conduct visits, and support trial execution while collaborating with cross-functional teams to maintain data quality. You’ll train site staff, foster strong site relationships, and drive continuous improvement in trial conduct. This role offers the opportunity to impact trial outcomes at scale within a diverse, inclusive environment.
Various annual leave entitlements
Health insurance offerings
Global Employee Assistance Programme LifeWorks
Life assurance
Country-specific flexible benefits such as childcare vouchers, gym discounts, travel passes
Monitor sites to ensure protocol adherence, regulatory compliance, and GCP standards
Conduct site visits to assess performance, resolve issues, and support trial execution




Collaborate with cross-functional teams for accurate data collection and reporting
Provide training and guidance to site staff and other CRAs to maintain high standards
Build and maintain effective relationships with site personnel and stakeholders to facilitate smooth operations
Bachelor's degree in a 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 with strong organizational and problem-solving skills
Expertise in monitoring practices, data integrity, and site management; proficiency in relevant trial software/tools
Excellent communication, interpersonal, and stakeholder management skills; ability to influence in a complex environment
J-18808-Ljbffr

📌 Senior Clinical Research Associate (Cusano Milanino)
🏢 Experteer Italy
📍 Cusano Milanino