Louise joined Illingworth in January 2016. She has over 20 years’ experience working in Scientific and Clinical Research. Louise has worked for a variety of companies in the Pharmaceutical industry – from a blue-chip Pharma, a large Biotech Company, to smaller Contract Research Organisations and more recently for a large Cancer Charity. During her Clinical Research Career, she has worked in several roles including: Drug Surveillance Officer, Clinical Research Associate, Clinical Operations Manager, Global Feasibility Manager & Clinical Study Manager.
Louise has worked in a variety of therapeutic areas across all phases of studies, specialising in Oncology. The varied companies and roles that she has worked for have enabled her to gain experience in all aspects of trial work such as project management, monitoring, protocol writing, CRF design, data management, ethics submissions and report writing. Louise has a proven track record of working on multiple projects and delivering to target. She has as strong commitment to quality and a reputation of being able to quickly develop people into productive, cohesive and motivated teams. Key to this are her effective communication skills and ability to clearly define expectations and responsibilities.