Overview In this role you will advance clinical studies by leading on-site and remote monitoring, ensuring data integrity and site partnership. You will drive study ownership across multiple sponsors and therapeutic areas, with a focus on deeper study knowledge and strong site relationships in Italy. You’ll mentor less experienced CRAs and operate in a trusted, autonomous setup. This is an international, cross-functional environment with meaningful impact on clinical trial success.

Retribuzione / Benefits

base salary range 41.000–51.900 gross annual salary premio incentive plans other benefits

Responsabilità

Conduct and report on-site monitoring visits and remote visits Perform CRF review,



source data verification and query resolution Manage site communications and relationships Participate in site identification Assist in training less experienced CRAs Lead assigned studies with ownership and cross-sponsor collaboration Support deeper study focus with fewer protocols in Italy

Requisiti fondamentali

College/University degree in Life Sciences or equivalent Independent on-site monitoring experience in Italy Experience in Phase II and/or III monitoring visits Full working proficiency in English Proficiency in MS Office Strong planning, multitasking and teamwork abilities Excellent communication, collaboration and problem-solving skills Ability to travel and hold a valid driver’s license communication collaboration problem-solving MS Office applications on-site monitoring CRF review

📌 Clinical Research Associate II (Milano)
🏢 Psi Cro
📍 Milano