since january 2016, i am working as Accounting assistant. during 4 years (from september 2009 until august 2013), i have worked in a Laboratory at jules bordet institute in the utch department/cord blood bank. i was Technician and also in charge of the qualtiy management (documents). in september 2007 (during 2 years), i was outsourced by a medical CRO/company to gsk Biological as cta in Vaccines department with all Compliance aspects and gcp. in september 2006 (during 1 year), i have worked as cta at quintiles in the start up department. i was in charge of all the administrative aspects of studies during start up phase: responsible for Ethics committee submission, collection of essential documents and reviewing translations of icf, synopsis and patient documents. before, during 10 years, i was Clinical data manager at erasme Hospital (brussels) in the anaesthesiology-reanimation department. i assisted the anaesthetists for clinical studies sponsored by Pharmaceuticals companies (9 clinical studies- Phase II to iv) and for academic studies. i have followed a lot of trainings on gcp, GMP and assisted in many inspections. __________________________________________________________________________________
AIDE ADMINISTRATIVE COMPTABLE MI-TEMPS
Since January 2016
Clinical Trial Assistant (CTA)September 2007 --- August 2009
Clinical Trial assistant (outsourced for dedevan) in malaria, dengue, and tuberculosis studies.
Clinical Trial Assistant (CTA)September 2006 --- September 2007
Clinical Trial assistant in the « start up group »: Clinical Trial submission to Ethics committee collection and administration of all essential documents coordination of activities administrative support to CRA for Planning selection visits internationals and nationals contacts check of the documents quality team work
Data Manager au service d'anesthésiologie_ErasmeSeptember 1996 --- September 2006
for anaesthesiology-reanimation department, full time (Professor barvais) sponsored Clinical trials: assist the anaesthetists in the data collection crf, complete crf (manually or on pc) and ec application forms, create study summaries, fill in sae reports, dispatching and archiving clinical documents, meet and answer CRA questions, maintain study files updated, creation of randomisation patients list, pre screening of patients list, track and program patient appointments, basic Statistics.
Graduate in cytology from De Mot Couvreur in 1995