Training content:- Planning and management of a clinical project- The regulatory aspects in terms of experimentation human rights, good clinical practices and the responsibilities of the clinical monitor during his various visits to the investigating physicians- Writing scientific documents relating to clinical studies- Mastery of data management and the functions of a data manager- Concepts in biostatistics for clinical trials and pharmaceutical research- The acquisition of the fundamental principles necessary for understanding pharmacovigilance- Knowledge and understanding of the relationships found between pharmacokinetics and pharmacodynamics

Project managementDevelopment of immunoassays based on flow cytometryI acquired experience in lateral flow immunoassay (LFA) and PCR combined to LFA.I acquired experience in validation, industrialization and commercialization of LFA diagnostic testsIVDR

. I have managed scientific projects and conducted experiments in human and animal immunology. My study has identified a new population of lung regulatory eosinophils. . Co-first author publications in the Journal of Clinical Investigation and several co-author publications. Oral communications. Surpersvision of PhD students. Member of the Belgian Immunological Society (BIS) and the Belgian Society of Physiology and Pharmacology (BSPP)

. I have conducted projects in lung immunology. My study identified the subset of lung dendritic cell responsible for airway allergic sensitization in mice. 1 co-first author publication (PlosOne) and 2 co-author publications. Expertise in animal models of airway allergy, flow cytometry and FACS sorting (professionnal training on FACS sorting by Becton Dickinson, Erembodeghem), ELISAs, cell culture, DNA and RNA extraction.Work in collaboration with industry (UCB).Member of the Belgian Thoracic Society (SBP-BVP) and Belgian Immunological Society (BIS)