12 ott - Roma
Altro
I am looking to connect with freelance clinical research associates who have experience in the monitoring of cardiovascular + medical device studies. You will be taking ownership of monitoring a single site, joining an already established team based out of Rome Italy, on a 12-month tempo parziale contract.
Key responsibilities:
Experience CRA with expertise in monitoring medical device clinical studies.
Conduct Source Data Verification and Source Data Review, ensuring data accuracy, and consistency with the EDC system.
Ensure compliance with study protocols, ICH-GCP guidelines, and applicable Italian regulatory requirements.
Manage and reconcile Trial Master File and Investigator Site File documentation to ensure accurate and complete site-level records.
Key requirements:
Fluent in Italian and with professional working proficiency in English.
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