James Hetrick, MPH

James Hetrick, MPH

  • Honorhealth Research Institute — Research Data Coordinator II
Research Division
  • Clinical Operations
Programs

Biography

James Hetrick is a Clinical Research Data Coordinator with a strong foundation in healthcare compliance and quality management. Currently serving as a Data Coordinator II at the HonorHealth Research Institute, James supports oncology research by managing complex clinical data in alignment with FDA regulations, ICH guidelines, and Good Clinical Practices. His expertise spans the collection, verification, and organization of clinical information and data in case report forms, liaising with sponsors, and contributing to the successful execution of pharmaceutical research study protocols.

Prior to his current role, James held key positions in accreditation and survey readiness at Blue Cross Blue Shield of Arizona and Health Choice Arizona, where he assisted in leading NCQA accreditation efforts and ensured organizational compliance across Medicaid and Medicare Advantage plans. His early career in behavioral health, including team leadership at a crisis stabilization unit, reflects his commitment to patient-centered care and operational excellence.

James brings a collaborative spirit, meticulous attention to detail, and a holistic understanding of clinical and regulatory environments to every project he undertakes.

Research Interests & Focus

James Hetrick’s research interests lie at the intersection of oncology clinical trials and data integrity. He is particularly focused on optimizing data collection and management processes to enhance the quality and efficiency of cancer research. His work supports the advancement of precision medicine through accurate data management, collaborating with sponsors and clinical teams, and rigorous adherence to FDA and ICH-GCP standards. James is also interested in the integration of real-world data into clinical trial workflows, the role of digital tools in improving protocol adherence, and the development of systems that support regulatory readiness and ethical oversight in clinical research environments.