A Medical and Clinical Affairs Expert encompasses strong scientific, informational, communication and interpersonal activities, and work with a range of different departments (e.g. marketing, regulatory affairs…) within the company in order to ensure maximum advancement of products in different stages of development.
Scope of project will include:
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Early phases clinical studies development
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Oversight of clinical trials strategy
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Medical Affairs strategy planning
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Representation of Medical Affairs vising within inter-company departments
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Communication with global regulators
Requirements:
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PHD or MD qualification
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Minimum 10 years experience in Medical and Clinical Affairs
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Expert knowledge of cardiovascular devices market
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Excellent knowledge of EU Medical Devices Regulations
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Experience in clinical trials design and strategy
