Lexi (Stefanie) Obara, BS, CIP


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

Regulatory and IND Management of Investigator Initiated Multi-site Trials