Lisa Cox has served in this role since July 2006; she joined the organization in December 1998 as a Sr. Clinical Research Associate.
Mrs. Cox has over 20 years of experience in clinical research. During her time at the CPC, Mrs. Cox has worked collaboratively to successfully implement a multi-center clinical trial management program. This has helped the Research Operations department move from monitoring and managing single-center clinical trials to managing global projects. Mrs. Cox collaborated with Dr. Hiatt and a dedicated team of CPC professionals to implement the Quality Intervention Program as a way to improve the collection of endpoint data in trials.
Prior to joining the CPC, Mrs. Cox worked for a Johnson and Johnson company, IRI Trial Management Center, Cato Research Ltd., and Pfizer, Inc. as a Clinical Research Associate. Mrs. Cox has experience conducting clinical trials in CNS, cardiovascular disease and oncology.
Mrs. Cox graduated from The Naropa Institute, Boulder Colorado in 1993 with a Master’s degree in Counseling Psychology.