Dr. Marisa Giro has a sound experience in clinical research from 1986. She works with pharma companies and CROs in monitoring and auditing international clinical studies. She has experience of co-monitoring in emergent countries, where she supports sponsors during the preparation and the conduction of inspections, and the implementation of action plans. She holds training on GCP and clinical operations activities, but also courses on communication techniques and work organization. She is active at ECCRT since 2009.