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I have more than 10 years of experience in the pharmaceutical industry. My writing services span the entire product lifecycle, ie from regulatory writing to market access-related documents up to medic
Nadia at a Glance:
I am a scientist with a Master of Science from the department of Ecology, Evolution and Behaviour at the University of Minnesota, and a versatile science communicator with more than 100 publications i
In the last 20 years, I was part of European Clinical Research teams involved in phase I to post-marketing pharmaceutical and device clinical trials.
I consider it to be a great opportunity a
Freelancer supporting clinical research activities and innovative projects with expertise and flexibility, locally and through Europe. Clinical Research Consultant providing services as Regulatory Sub
Results oriented multilingual Senior Consultant & Interim Manager, having first cumulated 40 years of managerial employments with major MNC's (Procter & Gamble ETC & Benelux, Monsanto Europ
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