Lexi has almost 20 years of research experience which includes investigator-initiated, multi-site trials involving investigational new drugs. The majority of her experience has been assisting investigators in conducting research, but she also has 6 years of experience as an IRB Administrator. Due to her extensive regulatory knowledge, she is a resource for Investigators and Coordinators, as well as for administrative functions such as editing protocols, informed consents, and standard operating procedures.

Cancer Focus