Email [email protected]
Lisa has been involved in the development of medicines and healthcare for over 20 years, starting as a research scientist in the pharmaceutical industry. After completing her PhD in medicinal chemistry, Lisa moved into business support roles.
In the past ten years she has broadened her experiences in the operational support of clinical studies. Lisa has undertaken global study management responsibilities in the oncology setting in pharma and has supported UK academic trials as trial manager for South Tees cardiovascular research.
Lisa’s role will provide project management support in enabling trials to be delivered to the highest standards within budget and timelines, and in adherence to UK clinical trial regulations.