Instructor Biographies
Michael Belotto, MPH, CCRC, CCRA
Michael Belotto is the Director of the BRANY Institute of Research Education. He also serves as a research compliance expert responsible for auditing sites to ensure investigators and investigator staff compliance with ethical and clinical guidelines and FDA regulations. He also serves on the BRANY Institutional Review Board.
Mr. Belotto was a paramedic in the New York City Emergency Medical Service for 10 years, with 7 years of experience in Hospital Administration.
Mr. Belotto is a graduate of New York Medical College where he completed a Masters in Public Health with a concentration in Epidemiology and Biostatistics.
Kimberly Irvine
Kimberly Irvine is the Executive Vice President of Operations and Regulatory of BRANY. Her responsibilities include coordinating and implementing business processes that enhance BRANY’s efficiency. Prior to her promotion to VP of Operations at BRANY, Kimberly was the Director of the Regulatory Department where her primary responsibilities were in Contracts and Budgets.
Ms. Irvine began her career in Healthcare Administration at the Weill Medical College of Cornell University and subsequently obtained a position as a Business Manager for the Department of Medicine at LIJ. She has 18 years experience in Healthcare Finance.
Ms. Irvine graduated with honors from St. Johns University in Healthcare Administration. She has co-authored a book on the Health Insurance Portability Accountability Act (HIPAA) called, “Ensuring a HIPAA-Complaint Informed Consent Process.”
Linda Reuter, MS, CIP
Ms. Reuter is currently working at the North Shore - Long Island Jewish Health System (NSLIJHS) as Director of the Huntington Hospital Institutional Review Board. Ms. Reuter has extensive experience in education and training related to the protection of human subjects in research, and is currently a member of two IRBs. She acts as a consultant for matters related to human subjects protection, and is currently teaching an online course related to health care infrastructure. She has over 16 years experience in the field of clinical research and IRB oversight and has trained many individuals in matters related to IRB regulations and oversight, informed consent, historical perspectives of IRB development, HIPAA, research ethics, compliance, etc. Her audiences appreciate her ability to take complex regulatory information and present it in an engaging and understandable manner.
Ms. Reuter has a B.S. in Biological Science and also graduated with top honors from SUNY Stony Brook with a MS in Health Sciences Research. She holds an Advanced Certificate in Health Care Management, and is a certified IRB Professional (CIP).
