Jeanna Julo

Jeanna Julo is a highly accomplished professional in the field of clinical research and healthcare compliance, currently serving as the Quality Improvement and Compliance Officer at the University of California, San Francisco’s Office of Clinical Trial Activation. In this pivotal role, Jeanna oversees the implementation of rigorous quality assurance protocols and compliance standards to streamline the initiation and conduct of clinical trials across diverse therapeutic areas, including oncology, infectious diseases, and biotechnology. Her expertise in Good Clinical Practice (GCP) and research compliance ensures that UCSF’s clinical trials adhere to regulatory requirements while maintaining the highest standards of research integrity and participant safety.

Jeanna’s strategic focus on quality improvement initiatives has led to the development of innovative workflows that enhance operational efficiency and facilitate faster trial activation without compromising compliance. She actively collaborates with multidisciplinary teams to optimize trial start-up processes, implement risk management strategies, and foster a culture of continuous quality enhancement. Her leadership in these areas supports UCSF’s mission to accelerate groundbreaking research and bring novel therapies to patients more effectively.

A recognized thought leader in the clinical research community, Jeanna has shared her insights at numerous industry conferences, including MAGI@Home, the Clinical Trials Innovation Programme, and MAGI’s Clinical Research Conference. Her presentations often highlight best practices in research compliance, innovative project management strategies, and the integration of emerging technologies in clinical trials. With certifications such as the Certified Healthcare Research Compliance (CHRC) and Certified Clinical Research Professional (CCRP), Jeanna combines technical expertise with practical experience, making her a vital contributor to advancing clinical research excellence at UCSF and beyond.