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.
📌 Freelance CRA / Italy - Roma, Lazio, Italy
🏢 Barrington James
📍 Roma
Candidati a questo annuncio
Mostra le tue capacità professionali all'azienda, compila il form e lascia un tocco personale nella lettera di presentazione, aiuterà il recruiter nella scelta del candidato.