Our Team

Kevin Bosse, PhD, RAC

Kevin Bosse, PhD, RAC
Director

Kevin Bosse, PhD, RAC, joined the Office of Research Regulatory Affairs (ORRA) in 2017. As a RAC-certified regulatory professional, he advises the development and regulatory strategy of novel drugs, biologics and devices under the Cellular Therapy and Cancer Immunology Program, as well as with other researchers both here and at The Ohio State University. With extensive project management, scientific and communications experience, Dr. Bosse assists through the full spectrum of regulatory submissions from preliminary meeting requests with the U.S. Food and Drug Administration (FDA) to Investigational New Drug (IND) and Investigational Device Exemption (IDE)filings and Centers for Medicare & Medicaid Services (CMS) coverage.

Previously, Dr. Bosse was assistant director of communications for Nationwide Children’s Hospital Foundation, helping to raise critical funds for the advancement of research and clinical programs at Nationwide Children’s. He holds a bachelor’s degree in Biology from Xavier University and a doctorate in molecular, cellular and developmental biology from The Ohio State University. Dr. Bosse completed a postdoctoral research fellowship at the Center for Cardiovascular Research.

Sue Marting

Sue Marting, MBA
Program Coordinator

Sue Marting brings over 25 years’ experience in regulatory affairs in the pharmaceutical, biopharmaceutical, device, food and personal care industries to Nationwide Children’s Hospital. She manages a wide ranging portfolio of regulatory filings for drugs and devices being developed for off-label or expanded access use at Nationwide Children’s Hospital and The Ohio State University.

Sue holds an associate of science degree in medical laboratory science from Mount St. Joseph University and is certified by the American Society of Clinical Pathology, a bachelor’s of science degree in business administration from Franklin University and a master’s of science degree in business administration with a concentration in finance and tax from Xavier University, and is Lean Six Sigma Black Belt Certified.

Kimberly Mattox

Kimberly Mattox, MS
Regulatory Project Coordinator

Kimberly Mattox, MS, joined the Office of Research Regulatory Affairs (ORRA) in 2022 as the regulatory project coordinator. She coordinates processing, reporting, record management and special projects for the department.

Prior to joining the ORRA team, Kimberly was the scheduling coordinator for the Clinical Therapies Department. Kimberly holds a Certificate for American Sign Language Interpreting from Columbus State Community College, a bachelor’s degree in Speech and Hearing Science from The Ohio State University, and a Master of Science degree in Applied Clinical Research Management and Regulatory Affairs from The Ohio State University.

Cory Hanlon

Cory Hanlon
Regulatory Specialist

Cory joined the Office of Regulatory Affairs as a regulatory specialist in 2021. He provides regulatory guidance and support for Nationwide Children’s Hospital Investigational New Drug (IND) and Investigational Device Exemption (IDE) applications to the U.S. Food and Drug Administration (FDA).

Prior to joining the team, Cory was a program coordinator in the Center for Perinatal Research. He holds a bachelor’s degree from the University of Cincinnati.

Elizabeth George

Elizabeth George, MS
Regulatory Specialist

In 2021, Elizabeth George, MS, joined the Office of Research Regulatory Affairs as a regulatory specialist to provide regulatory support for cell therapy products.

Elizabeth holds bachelor’s and master’s degrees in Biomedical Engineering and a master’s degree in Engineering and Management from Case Western Reserve University.

Angel Cinco

Angel Cinco, MPH, MD
Regulatory Specialist

Angel Cinco, MPH, MD, joined the Office of Research Regulatory Affairs in 2022 as a regulatory specialist. He supports submissions from the CONNECT program.

Previously, Dr. Cinco worked at Charleston Area Medical Center as a research review specialist then at OhioHealth as a human subjects protections consultant working close with the organization’s Institutional Review Board (IRB). Dr. Cinco holds bachelor’s degrees in Journalism and Biology from West Virginia University, a Master of Public Health degree in from Walden University and a medical degree from Gullas College of Medicine.