Overview In this role you will lead and execute clinical site monitoring for multiple studies within an international team. You will own study activities, maintain strong site relationships, and ensure data quality through CRF review, source data verification, and query resolution. You'll contribute to site identification and training of less experienced CRAs, while collaborating across sponsors and therapeutic areas. The position offers autonomy, scientific engagement, and growth in a dynamic, global environment.
Retribuzione / Benefits
base salary range 41.000 – 51.900 gross annual salary
premio
incentive plans
other benefits may apply
Responsabilità
Conduct and report onsite monitoring visits and remote visits
Perform CRF review, source data verification, and query resolution
Manage site communication and overall site oversight




Involve in site identification processes
Assist in training of less experienced CRAs
Take lead for assigned studies with ownership and autonomy
Requisiti fondamentali
College/University degree in Life Sciences or equivalent
Independent on-site monitoring experience in Italy
Experience in monitoring visits in Phase II and/or III
Full working proficiency in English
Proficiency in MS Office applications
Ability to plan, multitask and work in a dynamic team
Strong communication, collaboration, and problem-solving skills
Ability to travel and valid driver's license
communication
collaboration
problem-solving
multitasking
ownership
MS Office applications

📌 Clinical Research Associate (Italia)
🏢 Psi Cro
📍 Italia