Team Member

Alison has extensive practical experience of mammalian toxicology studies from a career with ICI Pharmaceuticals Division and the Central Toxicology Laboratory (latterly Syngenta) from 1982 until 2008. She was a highly experienced multi-disciplinary Study Director with a wide range of experience in the design, conduct, interpretation and reporting of a range of toxicology and safety pharmacology studies for both Syngenta and external clients.

During her career with ICI, Alison gained an Honours degree in Applied Biology. She then gained a post-graduate Diploma of the London School of Hygiene and Tropical Medicine and a Masters in Clinical Trials in 2013.

Within RSA, Alison is a Study Monitor working with a number of contract laboratories to deliver a range of Regulatory toxicology and environmental toxicology tests for clients. She is skilled in interpreting data, presenting facts clearly and in the liaison between the Laboratory and client. She has also worked with Laboratories to develop and improve templates for study plans and reports, on behalf of clients, to ensure clarity, consistency and regulatory approval.
acts clearly and in the liaison between the Laboratory and client.