Rebecca Carew is an experienced clinical research professional with over 18 years' experience in clinical operations, site monitoring, process development, training and auditing. She has a thorough understanding of GCP and ICH regulations, serving as GCP advisor and QA liaison. She has shown that she can manage internal and external teams, including multiple CROs and other vendors while contributing as team player and competent leader. She can identify training gaps, non-compliance issues and process improvement areas. She can develop training for internal and external teams, investigative sites, CRAs, venders and other areas.