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 clinical trial sites across the UK through qualification, initiation, monitoring, and close-out, ensuring patient safety, data integrity, and compliance with protocols and regulations. Maintain study documentation, support investigators and study staff, monitor site performance and investigational products, and collaborate with study teams to deliver trials successfully.
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.
