Richard Taylor Worth
About Richard Taylor Worth
Richard Taylor Worth serves as the Director of Quality Assurance at Evelo Biosciences in London, England, where he has worked since 2021. He has over 17 years of experience in clinical trials and quality assurance, having held various leadership roles in the pharmaceutical industry.
Current Role at Evelo Biosciences
Richard Taylor Worth serves as the Director of Quality Assurance at Evelo Biosciences since 2021. In this role, he is responsible for overseeing quality assurance processes and ensuring compliance with industry standards. His position is based in London, England, where he applies his extensive experience in quality management to support the company's objectives.
Previous Experience in Quality Assurance
Prior to his current role, Richard held several significant positions in quality assurance. He worked as the Director of R&D Audit and Inspection Management at Vertex Pharmaceuticals from 2020 to 2021. He also served as the Global Head of the Clinical Quality Evaluation Team and Senior Director of Global Clinical Operations (Quality) in various capacities from 2016 to 2020. His experience includes managing global teams and leading audit initiatives across clinical trials.
Educational Background
Richard Taylor Worth studied at Sexey's Grammar School in Bruton, Somerset, from 1977 to 1984. He furthered his education at the University of Roehampton, where he earned a Bachelor of Science degree from 1984 to 1986. He also attended the University of Buckingham from 1987 to 1990. His educational background provides a strong foundation for his career in quality assurance and clinical research.
Expertise in Clinical Trials
Richard possesses over 17 years of experience in monitoring and managing complex global clinical trials. His expertise spans various phases of clinical research, including Phase I-III trials, medical device studies, and nutritional studies. He has specialized skills in conducting Root Cause Analysis and designing Corrective and Preventive Actions (CAPA) training, which are essential for maintaining compliance in the pharmaceutical industry.
Leadership and Management Skills
Richard has demonstrated strong leadership and communication skills by managing global teams across different time zones. His experience includes designing and implementing Quality Management Systems crucial for maintaining high standards in clinical trials. He has led audit teams and conducted individual audits, showcasing a comprehensive approach to ensuring quality and compliance in clinical research.