The Clinical Research Associate will conduct site monitoring visits, ensure protocol compliance, and manage essential study documentation. They will also facilitate data query resolution and maintain strong relationships with investigative sites and study teams.
Manage investigative sites across Spain to ensure clinical trials adhere to study protocols, ICH-GCP, and regulatory standards. Responsibilities include conducting site visits, performing source data verification, and maintaining Trial Master File documentation.
Manage investigative sites across Italy to ensure clinical trials adhere to study protocols, ICH-GCP, and regulatory requirements. Perform site monitoring visits, verify source data, and maintain Trial Master File documentation while supporting study staff.
