Bio:
Melisa Williamson has over 14 years of experience working to improve efficiency and durability of processes within clinical research. Her experience spans multiple GXP environments, including managing and directing GCP Quality Assurance (QA) at various sponsors and CROs.
In her role at PharPoint, Melisa oversees quality initiatives within the organization and provides consultative support for sponsors navigating quality challenges.
Melisa is an experienced speaker within the clinical quality space with topics including Risk Based Quality Management (RBQM) and Quality by Design (QbD). She holds a BS in Biobehavioral Health at Pennsylvania State University.