Stephanie started her career in clinical data management in 2005 on the Contract Research Organization (CRO) side of the industry. She has since held various positions with increasing responsibility at CROs, pharmaceutical and in both large and small biotechnology companies.
She has a comprehensive knowledge of clinical data management from study set up through to regulatory submissions. She has extensive experience in vendor oversight, working with FSP models and managing outsourced data management teams.
She has experience in a wide range therapeutic areas including oncology, infectious diseases, immunology, neuroscience and rare diseases.
Stephanie joined the ACDM Conference Committee in 2020.