Matthew Tran
About Matthew Tran
Matthew Tran serves as a Senior Clinical Trials Assistant at Aimmune Therapeutics, where he has worked since 2018. He previously held research positions at UC Irvine, Genentech, and Affymetrix, and has a background in Biology from California State University-Monterey Bay.
Work at Aimmune Therapeutics
Matthew Tran has served as a Senior Clinical Trials Assistant at Aimmune Therapeutics since 2018. In this role, he has been involved in various aspects of clinical trial management. He has provided training for new Clinical Trials Assistants, ensuring they are well-prepared for their responsibilities. Additionally, he played a key role in the migration of the Clinical Trial Management System (CTMS) to a new platform, which included user access testing and data entry. His contributions support the efficient operation of clinical trials within the organization.
Previous Experience at UC Irvine
Before joining Aimmune Therapeutics, Matthew Tran worked as a Graduate Student Researcher at UC Irvine from 2015 to 2016. During his eight-month tenure, he contributed to research projects that enhanced his understanding of clinical research methodologies. This experience laid a foundation for his future roles in clinical trials and research assistance.
Experience at Genentech
Matthew Tran worked as a Research Assistant at Genentech for seven months in 2016. His role involved supporting research initiatives in a leading biotechnology company. This position provided him with valuable insights into the research and development processes within the pharmaceutical industry.
Educational Background
Matthew Tran studied Biology at California State University-Monterey Bay from 2008 to 2012, earning a degree in the field. He also attended the University of Missouri-Columbia, furthering his education. His academic background in biology has equipped him with a strong foundation for his work in clinical trials and research.
Administrative Support and Communication
In addition to his research roles, Matthew Tran has provided administrative support to the COVID-19 Response Team. His responsibilities included recording meeting minutes and drafting weekly newsletters, which facilitated effective communication within the team. He also organized and led the study team's annual Trial Master File (TMF) quality control process, ensuring compliance and organization in clinical documentation.