Experteer Overview As 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 / Benefits Monitor 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 Responsabilità Advanced 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, interpersonal, and stakeholder management skills Ability to travel at least 60% and valid driver's license Based in Rome, Venice and Florence area Requisiti fondamentali Annual leave entitlements Health insurance offerings Competitive retirement planning Global Employee Assistance Programme Life Works Life assurance Flexible country-specific benefits #J-18808-Ljbffr

📌 Clinical Research Associate (Italia)
🏢 Experteer Italy
📍 Italia