Our expert, Ms. Allecia Harley, will talk about the about the key components of a clinical research billing compliance program, common practices for creating a comprehensive program, creating a steering committee, and building the paper and electronic infrastructure to support it.
If you are new to research billing compliance, or are in the process of creating a program from scratch, this seminar will help you get started on your path. Attendees will receive a checklist to follow and a list of publically available resources to assist in creating the program.
Following are the session highlights:
Who should attend?
- Dr. David Lim
Allecia has 20 years of experience serving healthcare and higher education clients as an epidemiologist, researcher, administrator, and management consultant. She works extensively with clinical research executives in a variety of areas, including: budgeting, contracting; in-study management; policy, procedure, and template development; policy and procedure audits, and overall roles and responsibilities.
Allecia is a subject matter expert on research billing compliance and has conducted more than five hundred... More Info
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