✔Operational manager of the Application R&D team (12 scientists):Objectives:- produce scientific data demonstrating the power and capabilities of Syntax DNA printing system.- support marketing and sales with providing high level collaterals (Technical notes, webinars, posters etc...)- develop an automated gene assembly system (Syntax+Hamilton automate)- identify and develop innovative project on future products using EDS oligos (Enzymatic Synthesis).Results: see applications notes and webinar on DNA Script website✔Major partnering project manager.Full management of the research program for the American Defense Research Agency (DARPA) in collaboration with GE Healthcare:Objective: development of an integrated and automated workflow to produce thousands of ready-to-use vaccine doses. 5 years contract.Results: after 3 years, all milestones reached and deliverables provided in time.✔Coordinator of transversal activities within multiple teams- facilitate information sharing and communication across teams (synthesis , automation, bioinformatic, NGS, quality, product development, marketing and BD.- improve EDS oligo synthesis on Syntax system- support future product developments

Operation manager of the Research, Innovation, Bio-informatic, Manufacturing and Quality control teams.- Planning, cost control, identification and follow-up on milestones and deliverables- Responsible for product and services quality control and release.- CRO and service providers selection and management.

- Administrative, financial and operational management of clinical trials aiming at validating the in vitro Diagnostic Medical Devices (Multicenters, Europe). CRO and outsourcing control.- Clinical data analysis, communication and reporting (publication, posters, presentations)- Partner of the Quality Department to build regulatory technical dossiers (CE-IVD marking) and of marketing team for the launch of new products and services.

- Overall manager of project for clients with multiple studies and high budgets: activities coordination, project planning, phases and milestones identification, ressources management, budget control and invoicing, communication.- Responsible for an international team of Clinical Regulatory Consultants and management of european CRO.- Support to "Key Account Management" for commercial proposals and contracts on regulatory services.

- Operational, administrative and financial management of company clinical trials.- Full management of an international in vitro diagnostic medical device validation study in 17 centres and involving 1600 patients.- Management of CRO.- R&D Partner for trial design and result analysis

- Management/coordination of transversal projects (bio-informatics-therapeutics-genomics).- Management of pilot projects for new partners.- R&D team management.- Member of the strategic business development team.- Auditor of the Quality Management System- Member of the Intellectual Property Valorization working group.

- Management of the main scientific collaboration with Allergan: bio-informatic- genomic- therapeutic and medicinal chemistry team coordination; information, communication and reporting. -> New target and epitope discovery -> Research/development of new compounds entities.- R&D team management France+US.- Microarray product development and use for target discovery and biomarkers identification.

- Management of emerging projects using Exonhit proprietary technology (DATAS), collaboration and partnering with academic laboratories and pharmaceutical companies.- Development and optimization of the 1st generation microarrays (SpliceArrays).- Management of the technology optimization projects.- R&D team management.

- Full involvement in company founding (lab building and equipment, recruitment, training ...)- Development of the molecular biology technology patented by Exonhit: DATAS.- Development of a predictive toxicology product: SafeHit.

PhD in Molecular OncologyFrench government and ARC grants