Clinical Research Services
Clinical Research at CaroMont Health is comprised of two departments:
- Office of Research Administration
- Office of Human Research Ethics / Institutional Review Board(IRB)
Clinical research is subject to the regulations of the Food and Drug Administration
(FDA), and follows ethical and professional guidelines, including Good
Clinical Practice (GCP).
CaroMont Health currently has ongoing clinical trials in several therapeutic
areas, including cardiology and infectious disease, and oncology trials
offered through the CaroMont Cancer Center.
CaroMont Health Human Research Protection Program
Protecting the rights, safety and welfare of research participants at CaroMont
Health is our main priority. To accomplish this, CaroMont Health has in
place a Human Research Protection Program (HRPP) as we strive to exceed
the highest standards in clinical research.
Current, former, or potential research participants can contact the following
with questions or concerns regarding research at CaroMont Health. Research
compliance-related questions or concerns can also be addressed to the
Office of Human Research Ethics:
Institutional Official for Research, Office of Medical Affairs:
Research personnel are expected to report any known or suspected noncompliant
conduct related to research conducted at CaroMont Health. The confidential
CaroMont Health Corporate Compliance Hotline (
1-877.785.0001) is available for any individual that wishes to remain anonymous and/or
has found other reporting mechanisms to be ineffective.