Garth W.
About Garth W.
Garth W. is a Manager of Clinical Research at AVITA Medical, where he has worked since 2021. He has extensive experience in clinical trials, having held various roles at notable organizations such as Novartis and PRA Health Sciences.
Work at AVITA Medical
Garth W. has been serving as the Manager of Clinical Research at AVITA Medical since 2021. In this role, he oversees various aspects of clinical research, including the planning and execution of clinical trials. His responsibilities include managing trial budgets and conducting feasibility assessments for different sites. Garth's expertise in remote and virtual clinical trials enhances the efficiency of research processes at AVITA Medical.
Previous Experience in Clinical Research
Prior to his current role, Garth W. worked at Novartis for a total of four years, first as a Senior Clinical Research Associate from 2016 to 2019 and then as a Clinical Study Manager from 2019 to 2021. His earlier experience includes positions at inVentiv Health Clinical as a Senior Clinical Trials Associate and PRA Health Sciences as a Clinical Research Associate. Garth also worked as a Clinical Research Coordinator at UC Health and The Ohio State University Wexner Medical Center.
Education and Expertise
Garth W. holds a Master of Public Health (M.P.H.) degree in Health Policy & Management from Kent State University, which he completed from 2016 to 2018. He also earned a Bachelor of Science (BS) degree in Microbiology from The Ohio State University, graduating in 2007. His educational background supports his expertise in risk-based monitoring, vendor management, and digital patient recruitment strategies within clinical research.
Clinical Research Skills
Garth W. specializes in the planning and execution of remote and virtual clinical trials. He utilizes digital recruitment and site management solutions to enhance trial efficiency. His extensive experience includes managing clinical trials across various therapeutic areas, including rare and orphan diseases. Garth is also skilled in clinical trial budgeting and conducting feasibility assessments for different countries and sites.