I am currently working as a regulatory affairs officer and I am on the lookout for a new career direction.
I am particularly interested by the regulatory framework of medicines and health products, that’s why participating in the clinical development and market access of innovative products motivates me.
I am eager to develop my skills in regulatory affairs and ready for a new challenge.
Regulatory Affairs Officer
Since January 2015
• Writing marketing authorisation dossier for homeopathic medicinal products • Compliance with national and european regulatory frameworks • Reviewing scientific and legal documentations • Compiling modules 3 and 4 of the CTD • Participation in strategy meetings
February 2012 --- July 2014
• Clinical research: participation to the RAIDGBS project funded by the Walloon Region : development and validation of a new test for the rapid and easy identification of group B streptococcus in pregnant women • Quality Assurance : validation files and SOP writing for analysis that will be accredited by BELAC under the Standard ISO 15189 in the laboratory of infectious serology • Involvement to the activities and development of the National Reference Centers for Streptococcus agalactiae and mycoses • Evaluation and validation of new tests in bacteriology and molecular biology • Supervisor of microbiology practicals
October 2009 --- January 2012
• Development of a preclinical model of cystic fibrosis and characterization of in vivo efficiency of a new antibiotic treatment • Development of new therapeutic strategies against bronchial carcinoma
Analytical thinkingAttention to detailCollaborationSociabilityFlexibility
in Regulatory Affairs Manager from GIGA Biotechnology Training Center in 2014
Master's degree in Biomedical sciences from University of Liege in 2009