Tessa Clarke

Tessa Clarke has extensive experience in clinical research, currently serving as the Vice President of Quality at Catalyst Clinical Research since January 2017, with previous roles including Director of Quality and Compliance, Risk and Quality Lead, and Senior Clinical Project & Process Manager. Prior to this, Tessa worked as a Clinical Research Consultant from 2013 to December 2016, providing independent project management and medical writing services. Tessa's earlier roles include Research Prioritisation Consultant at NIHR Clinical Research Network and Senior Clinical Trials Development Manager at the Centre of Evidence Based Dermatology, focusing on Phase IV studies. Additional experience includes work as a Study Delivery Leader and CRA at AstraZeneca for various phase studies and as a Project Manager at Quotient Clinical Ltd. Tessa holds a degree in Biology and Environmental Science, Physiology from the University of Nottingham.