maintenantResponsible for the writing of the study documents from the protocol to the Clinical Study Reports in the oncology and inflammatory disease fields
Medical writing activities for preparing and submit protocols to AFSSAPS and Ethics Committee for clinical trials on medicinal products, and responses to health authorities questions
ABSCIENCE
maintenant
LFB
- Medical writer
2008 - 2010Experience working on CTD regulatory documents, especially in pediatrics, in the fields of immunology and homeostasis
Wrote Pediatric Investigation Plans for new medicine according to European regulation, clinical overview and summary
ADDS
- Clinical Research Associate
2008 - 2008Involved in the whole clinical study process, from protocol preparation to clinical trial monitoring, in a broad range of research fields.
Provided input in writing documents (epidemiology reports, protocols)
Ensure the monitoring of phase III clinical trials in oncology, neurology and neuropsychology
CNRS-BEAUFOUR IPSEN
- Doctoral Researcher
2003 - 2007Developed experimental and functional analysis methods to allow the use of microarray technology, in collaboration with Beaufour Ipsen company.
Research Subject : sarcopenia and the effect of a Ginkgo Biloba extract on striated muscle gene expression
