THE TEAM
An accredited specialist in Internal Medicine, and previous experience as a senior R&D executive with large pharmaceutical companies.
DR GRAHAEM BROWN
Founder
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Two decades of hands-on experience in clinical drug development and business management.
EVA HURST
Managing Director
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An experienced paediatrician
with over 15 years’ experience in research and development and medical affairs. If not working, he can be found on his gravel bike.
DR JOHN PORTER
Medical Consultant
Previous experience
as a senior executive in large pharmaceutical companies and a global CRO, with 30+ years' experience in international drug development. Specializing in gastroenterology, consults on CDDI’s projects.
DR JEAN-PIERRE ISAL
Medical Consultant
Senior executive with broad international experience in clinical and regulatory aspects of drug development both in large pharma companies and in small biotech companies.
DR MIKE TANSEY
Medical Consultant
Software Programmer
and tech guru on top of all data analyses and a key asset to all CDDI’s projects and daily
technological operations.
JEROEN VAN KESTEREN
EbF Technology
Former Research
Scientist with a PhD in
Molecular Biology and experience in Clinical Research, Manu combines scientific expertise with a keen sense of precision to guarantee the success of our clinical
projects.
MANUEL EGUREN, PhD
Clinical Project Manager
Having been a ball catcher at WImbledon, now Carolina catches vital information for our projects!
Regulatory document writer
and clinical operations manager with over 25 years’ experience in clinical research.
SUZANNE ALLEN
Clinical Project Manager
Clinical research project manager who works on all aspects of site management from initiation meetings, through monitoring to site close-out.
JENNIFER GROVE
Clinical Project Manager
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Experienced chartered accountant, using her know-how to promote financial success
and stability.
SUE BRAIN
Finance Director
OPENINGS
We are expanding and are looking for really smart physicians and other experienced clinical research professionals with drug development expertise, to work on a variety of novel projects. Broad, international experience of different therapeutic areas and phases is essential, and you must be able to confidently discuss protocol design with senior clinicians and site staff.
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If you are a talented programmer or data analyst, we would also like to hear from you.
Personal behaviour is paramount - excellent interpersonal communication skills; strong focus on delivering value to clients; personal commitment to targets; flexibility and openness to new ideas and methodologies.