What I do at MMV:
My role as Data manager consists of gathering data from clinical trials. The process of collecting and managing research data is done in accordance with regulatory standards to obtain quality information that is complete and error-free, the goal is to gather as much of such data for analysis as possible.
Why I work at MMV:
It is a great privilege to be part of the MMV team and to contribute to reducing the burden of malaria by developing medicines that are affordable for vulnerable populations. The biggest satisfaction is in knowing that my work has the potential to save the lives of children, who are the worst victims of malaria.
More about me:
Prior to joining MMV in 2020, I worked for 6 years as Clinical Data Manager for a Contract Research Organization. I started my career in preclinical research at Sanofi, Paris in the Safety Pharmacology department. In my professional career, I have amassed more than 15 years of pharmaceutical experience across pre-clinical and clinical development in the US and in Europe. I completed my Bachelors degree in Biology at Paris XII University in France.
Ask me about:
CDISC, SDTM, LOINC, data transfer, however I am also happy to discuss travels, tennis or places to go skiing in the Geneva area.