Diane is responsible for the management, planning and implementation of formative and summative research studies both directly for Team’s clients and as part of Team’s product development process. She is experienced in the implementation of HF studies involving administration of drug or placebo run under clinical protocols and the creation of HF documentation for US regulatory submission and response.
“What I enjoy most about my role is balancing softer interpersonal skills with the analytical mindset required to deliver great results for our clients. Designing and implementing HF studies is as much an art as a science, and crafting a good interview then analysing the results with clarity is extremely satisfying. Often the key skill lies in knowing what comments and input to ignore – of course I’m interested in learning what potential users think and feel about a product, but I work in the medical device arena so, above all, I’m focused on identifying and mitigating risk.”
“The regulatory requirement for robust human factors engineering in medical device development is well established. Team’s ability to deliver analytically as well as empirically – half of our HF group have first degrees in engineering – means that clients know they can rely on us to deliver thoughtful yet rigorous research with recommendations that are appropriate for the technology and manufacturing constraints.”
Diane has a degree in English Literature from the University of Cambridge. She has worked in user research since 2002, and has managed or contributed to dozens of projects involving various drug delivery and surgical devices, including inhalers, pen- and auto-injectors, transdermal and nasal delivery devices. In the past few years she has conducted over a thousand interviews with healthcare professionals and patients across a range of therapy areas including diabetes, asthma, Parkinson’s disease, hepatitis C, rheumatoid arthritis, multiple sclerosis and cystic fibrosis.