EXPERTISE

Kirsten Imbert – Van Harmelen has over 10 years of experience in the management of clinical trials across Europe and the US. Prior to becoming an independent clinical research consultant, she actively developed her expertise as an International Study Manager as well as a CRA in phase I-IV clinical trials for pharmaceutical, biotechnological, food and medical device companies, for both start-ups and industry leaders.

She holds a Master of Science in Nutrition and Health, specialized in Nutrigenomics and Toxicology, from Wageningen University in the Netherlands.

A solid expertise is built in project management and quality assurance in various therapeutic areas:

• Cardiovascular diseases
• Hepatology
• Hematology
• Endocrinology
• Metabolic diseases
• Infectious diseases
• Orthopedics
• Neurosurgery
• Respiratory diseases

KIRSTEN CLINICAL RESEARCH offers a side by side collaboration and is highly motivated to deliver a customized service corresponding to your timing, budget and quality expectations.

Your clinical trials can be managed in English, French and Dutch.

The proximity to Geneva and its international airport allows us to be rapidly present throughout Europe and other parts of the World.

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