Diane has a diverse background in toxicology that spans over 30 years working in the Central Toxicology Laboratories of Syngenta and within AstraZeneca.  Practical and Senior Investigatory roles and later as a Regulatory Project Manager with recognised specialism in reproductive toxicology and expertise with data interpretation, writing Common Technical Dossier tables, report summaries and auditing protocols and reports from CRO’s.  At AstraZeneca, Diane took the lead in one of the largest divestments’ worth in excess of $1 billion to raise funds for investment in new drugs.

As an experienced toxicologist, Diane is well versed with all aspects of Study Monitoring, with site visits, ongoing site dialogue and the review of study documentation whilst ensuring compliance with the appropriate regulatory guidance all within the framework of GLP. 

Experienced writer and reviewer of standard operating procedures (SOPs). She is skilled in Project Management, data analysis, problem solving and adapting communication styles to meet different cultures worldwide.