Holding a master’s degree in Biology and a Certificate in Clinical Research from Institute Léonard De Vinci in Paris, I have handled growing responsibilities with my first experience as a Study Coordinator. Actually, I am part of a clinical trial team and responsible to make sure that rights and well-being of subjects are protected and also that a quality control of clinical data are accurate, complete and verifiable from source documents during a trial. My numerous responsabilities as a Study Coordinator have allowed me to develop communication skills and thus to work efficiently as a team member .I have also had the opportunity to acquire leadership qualities. With my strong management and organizational skills, and my ability to adapt to new environments.I will be quickly independant and operational.
Excellent knowledge of regulations and clinical practices as defined by the International Conference of Harmonisation Recommendation on the content of the Trial Master File and Investigator Site File
