Scot Davies
About Scot Davies
Scot Davies is a Clinical Endpoints Specialist currently working at MeiraGTx in London, England. He has over a decade of experience in clinical project management, including roles at Kantar Health and Cancer Research UK, and possesses expertise in contract negotiations and regulatory submission processes.
Work at MeiraGTx
Scot Davies has been serving as a Clinical Endpoints Specialist at MeiraGTx since 2021. Located in London, England, he is responsible for overseeing clinical endpoints in various projects. His role involves ensuring that clinical trials meet regulatory standards and that endpoints are clearly defined and measured. This position builds on his extensive experience in clinical project management.
Previous Experience in Clinical Project Management
Prior to joining MeiraGTx, Scot Davies worked at Kantar Health as a Senior Clinical Project Manager from 2012 to 2018. During his tenure, he managed clinical projects and collaborated with various stakeholders in the healthcare sector. He also held a position at Cancer Research UK as a Clinical Project Manager from 2006 to 2011, where he contributed to significant research initiatives. His earlier roles include working at Synarc and the University of Surrey, where he gained valuable experience in project management.
Education and Expertise
Scot Davies has a solid educational background in the sciences. He studied Biochemistry at North East Surrey College of Technology, achieving a Higher National Diploma (HND). He also completed studies in Applied Biology and graduated from the Institute of Biology. His foundational education includes O and A levels from Cornwall Technical College and CSEs from St Ives Secondary Modern School. This academic background supports his expertise in clinical research and project management.
Specialization in Clinical Trials and Vendor Management
Scot Davies possesses extensive experience in managing Investigator Initiated Trials (ITT) and studies involving medical devices. He has a strong background in contract and budget negotiations with NHS Trusts and Boards. Additionally, he has experience in vendor management, working with Clinical Research Organisations (CROs), biotechnology companies, and pharmacokinetic/pharmacodynamic analytical laboratories. His knowledge includes the submission process requirements of regulatory bodies such as the Health Research Authority (HRA) and the Medicines & Healthcare products Authority (MHRA).
Background in Clinical Research
Scot Davies has over ten years of experience working in the ADME and Enzymology groups within a Clinical Research Organisation. His career in clinical research began in the early 2000s, and he has since developed a comprehensive understanding of the clinical trial process, regulatory requirements, and the management of complex research projects. His diverse experience has equipped him with the skills necessary to navigate the challenges of clinical endpoints and project management.