OUR MANAGEMENT TEAM
With extensive experience in clinical research, I've built a reputation for a calm, diligent and professional approach, consistently delivering high quality outcomes in numerous drug development organisations. My diverse experience spans roles in pharma, biotech and academic/not-for-profit settings. I am passionate about access of paediatric patients to safe and effective therapies, and the safety and well-being of paediatric study participants throughout the drug development process. Unusually in this industry, I've worked in leadership roles across many Clinical Development functions, including Clinical Operations, Data Management, Quality, Regulatory and Pharmacovigilance. My involvement covers all stages of the development lifecycle, from trial design and setup to study oversight, close-out and reporting.
I undertook my medical training at Cambridge University and have been in the pharmaceutical industry for more than 27 years. I have extensive experience in clinical development and medical affairs across many therapeutic areas, including oncology, supportive care, peri-operative medicine, anti-infectives, and neurology. With over a decade of leadership in R&D for a successful start-up operating in the US and Europe, I have comprehensive practical knowledge of the entire drug development process, covering strategic planning, regulatory affairs, clinical science and clinical operations, with specific insight into the challenges facing smaller companies. Among my specialist areas of expertise are paediatric drug development, drug repurposing and 505(b)(2) and mixed/hybrid development programmes.