A wealth of experience in both Pharma and the CRO environment

Diane has been in the industry for 30 years and has a wealth of experience in both Pharma and the CRO environment as well as having been a Director of her own successful consulting company.

Diane has worked across the globe including Poland, the USA, the UK and Switzerland covering all phases of clinical research. Her experience in QA includes for-cause audits and acting as a sponsor representative for a successful FDA Inspection.

At CPR her highly skilled team includes both Clinical and Analytical QA Managers.

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