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• Researcher in Virology group, University of Tampere (asthma, rhinoviruses, hygiene hypothesis, RT-qPCR)
• Customer service experience from >10 years
• Interested in event organizing and net
Working in a CRO I am the clinical regulatory affairs referent for European projects. I have a sound experience dealing with Clinical Trial Applications (CTA) both to competent authorities (CA) and et
Free-lance with over 25 years of experience in medical dept of pharmaceutical industries and global/national CROs
Creating entrance in new markets, building strong indepth KOL relationships, cross functional leading skills. Startup of Investigational Initiated Trials (IIT’s or IST's) Broad network in Dutch and B
Professional Objective: Looking for a Regulatory affairs position in CMC
After an education in biochemistry and chemistry, I hold a PhD degree in biotechnology. I gained relevant and various academic
• Clinical Research Professional with 9 years' experience in clinical development in pharmaceutical/biotech industry, CROs and academia• Expertise area in early clinical developm
R&D Quality Assurance Professional, Clinical Trials Auditor, Root Cause mapping specialist and Risk-based thinker, always interested by QA leadership and/or Auditing opportunities in Europe or Nort
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