Keeps abreast of scientific, regulatory and operational aspects of projects.
Assists site selection, initiation visits and startup documentation.
Conducts monitoring visits; ensures CRF accuracy per protocol and ICH-GCP.
Performs source data verification and in-house data review; resolves data queries.
Manages investigational products and trial materials; ensures supply.
Main site contact; supports safety reporting and follow-up with sites.

🎯 Requirements

University Degree in scientific medical or paramedical disciplines.
Proven experience as a CRA with on-site monitoring.
Experience with Italian ethics committee submissions.
Strong knowledge of GCP/ICH Guidelines and regulatory requirements.
Fluent in English and Italian.
Proficiency in Microsoft Office; willing to travel.

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