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Clinical research billing (CRB) programs are required for all organizations participating in clinical research activities. This programs require the full understanding and application of applicable federal and state regulations governing clinical research activities. To be successful, organizations participating in clinical research activities should leverage technology to drive the daily operations and mitigate risk of non-compliance. The current complexity of the clinical trials requires innovation and optimization of technology platforms like the electronic health record (EHR).
Learn best and leading practices around optimizing and leveraging technology to build a compliant clinical research billing program.
Mary Veazie is a CPA and seasoned clinical research finance expert with more than 20 years of experience serving as the interface between principal investigators, clinical operations, and executive leaders in order to drive the development and implementation of clinical research program initiatives. Over the course of her career, she has been an innovative healthcare leader with a unique perspective in managing the financial aspects of the clinical research enterprise. She brings extensive experience in financial program management, financial modeling, and business plan development within the clinical trial space. Mary has a strong understanding of federal and FDA regulations governing the life sciences industry which has made her successful at leading initiatives and business transformation projects.
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