Mariana MÜLLER

Monitor of clinical trials being conducted in Spain and UK, in join effort with the CRAs, acting as the mainline of communication between the Study lead and the investigational site. Site management, supervision and support.

CRA for all sites taking part in an Observational Study (Phase IV) in Argentina. Manage all activities of the Non-Interventional Study in the assigned centres. Perform on-site visits, CRF reconciliation, training, and all monitoring related-tasks.

In-House (remote) monitoring of investigational sites located in several Latin American countries. The primary point of contact for the site staff during the study start-up activities, the conduction of the study, or the close-up period. Provide support, supervising the compliance to Protocol and GCP and assisting them in all study-related tasks.