Maxwell Miller

About Maxwell Miller

Clinical research professional with experience monitoring phase I, II, and clinical trials. I have experience conducting all visit types in the indications of cardiology, gastroenterology, hormonal/metabolic disorders, and obstetrics/gynecology in pharmaceutical and medical device studies. l have obtained advanced monitoring certifications for rare disease and medical device monitoring, along with completing the PACE CRA training program. University of Cincinnati Alumnus, where I studied Biomedical Engineering with a focus on medical device design. Throughout my undergraduate career, I became an active member on campus and within university athletics. As a graduate, I work to stay involved with my community, and to give back to the programs and people that have helped to build me thus far.

Experience

1. Clinical Research Associate

   ICON plc

   Jan 2026 — Present

   Conduct routine monitoring visits, including site qualification, initiation, monitoring, and close‑out activities- Ensure study sites adhere to protocols, regulatory standards, and ICON/Sponsor expectations- Perform source data verification and ensure data integrity, accuracy, and timely query resolution- Build strong, professional relationships with site staff to support enrollment, troubleshoot issues, and maintain study momentum- Prepare detailed monitoring reports and maintain essential trial documentation- Identify risks or protocol deviations and implement corrective and preventive actions- Collaborate closely with project managers, clinical leads, and cross‑functional teams to support study timelines and deliverables- Contribute to continuous improvement by sharing operational insights and supporting process optimization.

Education

• University of Cincinnati

  Bachelor of Science - BS, Biomedical Engineering

  2017 — 2022

• Centerville High School

  High School Diploma