Adrianne Phillips has over eight years of research experience spanning quality assurance, clinical operations, clinical development, and regulatory affairs. She has supported numerous clients by providing expertise in quality management system assessment and development, clinical quality compliance oversight, project and program management, inspection readiness analysis, remediation and support, clinical document development, and regulatory authority submission preparation and communication. She has worked across all stages of the development life cycle and within multiple therapeutic indications, including numerous oncology indications and rare disease such as ALS and Graft versus Host Disease (GvHD), with experience in bi-specifics, monoclonal antibodies, and gene therapy as well as healthy volunteer studies.