Direct and Supervise activities related with clinical trials, its development since startup until the clos: Feasibilities, study budgets, staff training, local quality control overall the project, local clinical monitoring, regulatory task.
Participate in projects desing as clinical psychologist and expert on operational manager of clinical projects.
Lead clinical operations for the selection of study coordinators, investigators as well as his/her training.
Training on CGP and Clinical Research for external groups, as well as training for site satff (study coordinators, investigators, nurses...)