Extensive experience in in-vitro ***** (IVD) Project and Product management (concept & design, budget & personnel management, clinical trials, scale-up, transfer to production, regulation (CE-IVD, FDA 510(k)), and post-market troubleshooting). Skilled in negotiating joint co-operations with biotech companies, academic research institutions and TTO's. Experienced in allocating, contracting and management of distributors worldwide. Deeply experienced with raising external grants. Conducted several strategic evaluation rounds of new projects (Market research and feasibility and profitability analysis). Possesses deep working knowledge in the global IVD market in terms of major players, trends, regulatory requirements, channels of distribution and re-imbursement policies.

General: Lead and motivate peers and co-workers to realize goals of projects, experimental design, troubleshooting, data-analysis and logical interpretation of results. Focused and task oriented. Capable of working independently and as part of a team. Substantial written and oral presentation skills. Co-authored book chapters and scientific reviews. Authored scientific papers in peer-reviewed journals. Presented research work in numerous national and international scientific meetings and workshops