Tina Lechman, Senior Clinical Project Manager, has been with SPR Therapeutics since the company’s inception in 2010. Prior to joining SPR, Ms. Lechman spent over 6 years in her roles as a Clinical Project Manager and Sr. Clinical Project Manager at
NDI Medical, the parent company of SPR, where she oversaw clinical study activities, monitored studies for compliance with Good Clinical Practices, and contributed to various FDA regulatory submissions. Prior to joining SPR Therapeutics and NDI Medical, Ms. Lechman served as a Clinical Studies Coordinator for a neurostimulation device company where she completed a multicenter clinical study and contributed to the FDA Humanitarian Device Exemption approval for a Class-III implantable neurostimulation device. In addition to her industry experience, Ms. Lechman has also has worked for an independent Contract Research Organization and a Washington-based regulatory consulting firm, both which served high-profile medical device and pharmaceutical clients. Ms. Lechman has over 13 years of experience in the medical device industry, with nearly 10 years of clinical research experience specifically dedicated to neurostimulation devices. Ms. Lechman earned a bachelor’s degree in biology from Allegheny College in Meadville, PA.