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312.463.6222
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FDA

Erik A. Martin

Erik Martin is dedicated to providing effective, efficient and innovate solutions to health care clients. He focuses on health care regulatory compliance matters, operations and transactions. He works closely with academic medical centers and health care providers to advise them in areas of clinical research billing compliance, developing health care system compliance policies and regulatory materials and drafting system wide contracts and services agreements. Erik’s experience includes working with non-profits on health care and financial regulatory matters and implementing federal health care regulations at the state level and developing and conducting client training programs related to clinical research billing, healthcare operations, and various other healthcare compliance and regulatory matters.

He previously specialized in clinical research matters, and he has worked on all aspects of clinical research on the institution and provider side. He has also built and managed a team of about 45 consultants working across several projects and specialty areas. Erik has helped several of the largest academic medical centers in the country as well as a number of community hospitals and physician groups develop (or rebuild) clinical research management and billing compliance programs, create and implement research policies and procedures, operationalize regulatory controls, draft and negotiate clinical trial agreements, and work with all stake-holders (e.g. investigators, study teams, legal, billing, IT, etc.) to develop buy-in and cohesion.