Lisa Luttinger has over 20 years of experience in the medical device industry and has contributed to over 25 studies throughout her career. Her venture into the clinical operations field was first in an administrative capacity but then slowly developed into a passion for clinical trial management which was cemented while attaining a certificate in Clinical Trial Design and Management from San Francisco State University. Throughout her tenure at Cerus, Lisa expanded her contribution to the clinical operations department with her knowledge of cross-functional teams including Regulatory, Legal, Data Management, Quality Assurance, Accounts Payable, and Marketing all of which she uses in her current role as a Clinical Trial Manager.  Of note is her critical role in managing multiple FDA e-submissions for two approved products.   She also has experience preparing sponsors and investigational sites for FDA (BIMO) Audits and a high proficiency of the DIA model for Trial Master Files.

 

When Lisa isn’t working on a study, she enjoys acting in local community theater, volunteering for charitable organizations, and traveling, which allows her the opportunity to meet new people.