Brittany Scott

Brittany Scott is a seasoned professional in clinical operations and regulatory affairs with extensive experience in study start-up and project management. Currently serving as Lead Site Activation Officer at Allucent since September 2022, Brittany develops management plans in collaboration with the Global Regulatory Manager, ensuring compliance with local regulatory documentation for clinical trials. Previous roles include Study Start-Up Associate at ICON plc, where Brittany contributed operational expertise, and Clinical Operations Specialist at Genentech, fostering collaboration across various departments to streamline clinical trial delivery. Brittany has a solid background in preparing and negotiating clinical trial agreements while maintaining thorough knowledge of ICH, FDA, IRB, and GCP guidelines. Brittany holds a Bachelor's degree in Sociology with a minor in Women & Gender Studies from the University of North Carolina at Charlotte.