Skip to main content

The Clinical Research Compliance Office (CRCO) is a unit of the Office of the Vice Chancellor for Research, Research Compliance Services committed to partnering with the research community to promote innovation and effectiveness while upholding a strong compliance program. The CRCO aligns with UNC-Chapel Hill’s mission to advance scientific knowledge and protect the rights, safety, and well-being of research participants locally, nationally, and internationally. We achieve this by:

  • Supporting Sponsor-Investigators throughout the lifecycle of drug, device, and biologics development.
  • Conducting post-approval reviews of clinical studies through the Clinical Trials Quality Assurance (CTQA) program.
  • Ensuring compliance with ClinicalTrials.gov registration and results reporting.
  • Engaging collaboratively in policymaking and program implementation to ensure adherence to federal, state, and institutional requirements.
  • Supporting the clinical research community with comprehensive compliance education and resources.
  • Serving as a central point of contact for clinical research compliance matters.

Contact our Teams

If you have any questions, feedback, or need support, our team is ready to help!


Meet our Team



Headshot photo

Jeanne Lovmo

Associate Director
Policy and Governance
lovmo@unc.edu


Headshot photo

Monica Coudurier

Clinical Trials Project Manager
ClinicalTrials.gov
m_coudurier@unc.edu


Headshot photo

Jamie Kauwell

Director
Clinical Trials Quality Assurance (CTQA)
jamieb@email.unc.edu
919-966-2031