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-18808-Ljbffr

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