Ea Marie Holst is a Partner at Pharma IT, a pharma-focused consultancy that assists its clients across all key areas within the pharmaceutical, biotech, and medical device industries. As a seasoned pharmacovigilance professional with 15 years of experience in the pharmaceutical and medical device industries, she leads the firm’s pharmacovigilance team. Ea has worked in both headquarters and affiliates with all aspects of post-marketing pharmacovigilance and clinical study safety including; Risk management, external and internal Data Monitoring Committees, Signal detection, benefit-risk evaluation, building and maintaining quality management systems, Pharmacovigilance training, E2b reporting and testing, literature monitoring, ICSR case processing and reporting, reconciliation and coding in clinical trials, complaint and medical information handling and reconciliation. She is GCP certified, as well as trained in Argus Safety and ARISg™.