• Many years of clinical practice in Internal Medicine and 30 years of experience in the Pharmaceutical Industry with ability to work in almost any therapeutic area
  • Flexibility required to work successfully with the large multinationals, medium sized companies and the smallest biotechs
  • Preparedness to contribute to and become part of the team, so vital for successful development and registration of new medicines
  • Ability to analyse the issues whether they be related to identifying the clinical target, design of clinical trials, planning the exploratory development, establishing proof of concept, handling safety of trial subjects, addressing regulatory concerns or identifying the strengths and weaknesses of a development pipeline
  • Interpretation of data and integration of information to identify the strengths and weakness of a drug development programme and applying these to registration
  • Writing high quality documents, expressing the critical arguments clearly
  • Accustomed to working in a global environment with clients based in USA, Japan and Europe
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