UC Davis Health
Rancho Santa Margarita, California
Laura is an experienced Regulatory Compliance Analyst at the CTSC Clinical Trials Office (CTO). She leads the CTO Regulatory Team and is responsible for overseesing and managing the CTO regulatory portfolio, which includes over 30 departments in multiple medical indications. As a skilled analyst, she integrates effective workflows to maiximize outcomes on initial start up submssions all the way through closure of studies.
Laura first joined the UC research community at the Irvine campus in 2003 as a Bilingual Clinlcal Research Coordinator for the Chao Cancer Family Center. After working as a Clinical Research Coordinator she joined the private sector and worked for Pharmaceutical / Biotech companies and a mid-sized CRO before returing to the academic clinical research sector at UC Davis Health in 2017.
As an experience Regulatory Compliance Analyst, Laura brings unique perspectives gained from her work at Academic Research Institutions, Clinical Research Organizations (CRO) and in the pharmaceutical sector. She earned her Master's in Healthcare Administration from the California State University, Long Beach and is a Certified CRC through the Association of Clinical Research Professionals. Her strong background in process improvement, development and managing a diverse regulatory portfolio adds to her proficient skills in the clinical research community.
D13 - IRB Process Improvements: Collaborative Methods With Institutional Clinical Research Liaisons
Wednesday, December 14, 2022
11:45 AM – 12:45 PM ET