Lizette C.

Lizette C. is an accomplished project manager with extensive experience in clinical research and regulatory compliance. Currently serving as a Project Manager at George Clinical since February 2023, Lizette previously held the position of Associate Project Manager at Translational Drug Development (TD2) from August 2021 to February 2023. Prior roles include Senior Country Approval Specialist at PPD and various positions at Mayo Clinic, including Regulatory Protocol Specialist focused on Phase 1/Early Cancer Therapeutics, and Cancer Clinical Research Coordinator (CCRP). Lizette has a strong background in managing multi-site clinical trials, coordinating research document compliance, ensuring adherence to FDA regulations, and overseeing operational responsibilities at clinical study sites. Lizette holds a Bachelor of Science in Biochemistry from Arizona State University and a Master of Business Administration (MBA) with a concentration in healthcare management from the University of Phoenix.