ppI 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.
/p h3Key responsibilities: /h3 ul liExperience CRA with expertise in monitoring medical device clinical studies.
/li liConduct Source Data Verification and Source Data Review, ensuring data accuracy, and consistency with the EDC system.
/li liEnsure compliance with study protocols, ICH-GCP guidelines, and applicable Italian regulatory requirements.
/li liManage and reconcile Trial Master File and Investigator Site File documentation to ensure accurate and complete site-level records.
/li /ul h3Key requirements: /h3 ul liFluent in Italian and with professional working proficiency in English.
/li /ul /p #J-*****-Ljbffr

📌 Freelance Cra / Italy (Lazio)
🏢 Barrington James
📍 Lazio