Senior Clinical Research Associate

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/781gog

ppExperteer OverviewAs 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. /ph3Retribuzione / Benefits /h3ulliMonitor trial sites for protocol adherence, regulatory compliance,



and GCP /liliConduct site visits to evaluate performance and resolve issues /liliCollaborate with cross-functional teams for timely data collection and reporting /liliProvide training and guidance to site staff and other CRAs /liliBuild and maintain effective relationships with site personnel and stakeholders /li /ulh3Responsabilità /h3ulliAdvanced degree in a relevant field such as life sciences, nursing, or medicine /liliExtensive experience as a Clinical Research Associate /liliProven ability to manage multiple sites and projects /liliExpertise in monitoring practices, data integrity, and site management /liliProficiency in relevant clinical trial software and tools /liliExcellent communication, interpersonal, and stakeholder management skills /liliAbility to travel at least 60% and valid driver's license /liliBased in Rome, Venice and Florence area /li /ulh3Requisiti fondamentali /h3ulliAnnual leave entitlements /liliHealth insurance offerings /liliCompetitive retirement planning /liliGlobal Employee Assistance Programme LifeWorks /liliLife assurance /liliFlexible country-specific benefits /li /ul /p #J-18808-Ljbffr

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/781gog