Lisa Cox joined CPC in 1998 and has been the driving force behind making CPC Clinical Research a prestigious academically led CRO. In her current roles as Chief Operating Officer and Director, Clinical Research, Ms. Cox’s leadership ensures that CPC remains at the forefront of excellence from both business and research perspectives.
Ms. Cox brings over 30 years of experience in clinical trials from a variety of roles and types of organizations including pharmaceutical companies, contract research organizations, study sites, and university/academic settings. This robust and diverse background uniquely positions her to lead CPC with a rich perspective that provides solutions incorporating everyone’s best interest. Ms. Cox provides direct oversight to the departmental/functional leads and actively supports our research project teams to help identify and mitigate potential study risks.
One of her many contributions to CPC includes spearheading the inception and development of the Endpoint Quality Intervention Program (EQuIP®) that has reliably shown decreased variability in functional endpoint data.
Ms. Cox received her Master’s degree in Psychology from The Naropa Institute, Boulder Colorado.