Sr. clinical research associate

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7hw9xf

Experteer Overview As a Senior CRA at ICON, you oversee clinical trial activities to ensure protocol adherence, regulatory compliance, and data integrity. You will support site visits, train staff, and collaborate with cross-functional teams to drive smooth trial execution. The role is pivotal in safeguarding participant safety and trial quality across sites and studies. You will work within a diverse, inclusive culture that values excellence and impactful clinical development. Retribuzione / Benefits Monitor trial sites for protocol, regulatory, and GCP compliance Conduct site visits to assess performance and resolve issues Collaborate with cross-functional teams to ensure timely data collection and reporting Provide training and guidance to site staff and other CRAs Build and maintain relationships with site personnel and stakeholders to enable smooth operations Responsabilità Advanced degree in a relevant field (life sciences, nursing,



or medicine) Extensive experience as a Clinical Research Associate with strong regulatory knowledge Ability to manage multiple sites and projects with organizational and problem‐solving skills Expertise in monitoring, data integrity, and site management; proficiency with clinical trial software/tools Excellent communication, interpersonal, and stakeholder management skills; capable of driving compliance in a complex environment Ability to travel at least 60% with a valid driver's license Requisiti fondamentali annual leave entitlements health insurance offerings retirement planning options Global Employee Assistance Programme Life Works life assurance flexible country‐specific optional benefits #J-18808-Ljbffr

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7hw9xf