Email: [email protected]
Dr. Chris Longspaugh, a pharmacist with a varied career, has over 20 years of experience in multiple areas of clinical research including: billing compliance, clinical trial operations, information technology, and project coordination. Most recently Chris served as Senior Manager of Medical Operations of a mid-sized biotech company where he was responsible for clinical trial budgeting and forecasting, strategic planning and key opinion leader endeavors. Chris spent over 8 years at the University of Southern California leading a team conducting prospective clinical trial coverage analyses and as a member of the management team he produced operational, budgeting and financial trial reporting tools utilized by the institution. Chris has presented on topics including: Clinical Trial Policy / NCD 310.1, investigator initiated research, clinical trial budgeting and billing processes, routine costs in clinical trials and research compliance.