Ben Mooso, MS, CCRP

Director, Office of IRB Administration

UC San Diego

Ben Mooso started in Clinical Research in 2013 when he began working for the IRB at the Sacramento VA. There, he began his knowledge journey in both the IRB and Clinical Research worlds, learning about clinical trial conduct and regulations. In 2014, he started as a Regulatory Analyst in UC Davis’ Emergency Medicine department, where he learned to manage clinical trials, enroll subjects, process data and specimens, all while further honing his skills in the regulations that surround Clinical Research. In 2018, he became the Associate Director for the IRB at UC Davis, where he leveraged his knowledge of the clinical trial lifecycle to ensure a quality experience for both researchers and clinical trial participants. In 2021, he became the Director for the IRB at UC San Diego, where he has worked to increase efficiencies while still maintaining a high standard of safe and ethical conduct in the Clinical Research space.

Sessions

• Demystifying Institutional Review Board Structures and Processes

• How the New Single IRB Requirements Will Change Clinical Research

Watch Sneak Peeks into Ben’s Session Content