Freelance CRA / Italy

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/8i5enm

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.

If interested, please email me at (email hidden).

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/8i5enm