Senior Clinical Research Associate
Pubblicato il 25-08-2026 - Experteer Italy in Cusano Milanino
ppAs 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. /pulliVarious annual leave entitlements /liliHealth insurance offerings /liliGlobal Employee Assistance Programme LifeWorks /liliLife assurance /liliCountry-specific flexible benefits such as childcare vouchers, gym discounts, travel passes /liliMonitor sites to ensure protocol adherence, regulatory compliance, and GCP standards /liliConduct site visits to assess performance, resolve issues,
and support trial execution /liliCollaborate with cross-functional teams for accurate data collection and reporting /liliProvide training and guidance to site staff and other CRAs to maintain high standards /liliBuild and maintain effective relationships with site personnel and stakeholders to facilitate smooth operations /liliBachelor's degree in a relevant scientific discipline or healthcare-related field /liliExtensive experience as a Clinical Research Associate with strong understanding of trial processes and regulatory requirements /liliProven ability to manage multiple sites and projects with strong organizational and problem-solving skills /liliExpertise in monitoring practices, data integrity, and site management; proficiency in relevant trial software/tools /liliExcellent communication, interpersonal, and stakeholder management skills; ability to influence in a complex environment /li /ul /p #J-18808-Ljbffr