and result-oriented pharmaceutical
professional with more than 5 years experience in post marketing pharmaco-epidemiological
studies and pharmacovigilance.
CHILTERN (on behalf of Novartis/Sandoz)
Clinical Research Associate II for Late Phase Studies in
Rheumatology, Epidemiological Studies
Nov 2017 to
Assist and collaborate in the contractual
financial agreement realization, performing site
monitoring and site selection visits.
January 2015 to January
Managing several clinical study sites
(Phase 4), to ensure surveillance for assessing the safety profile of the
subcutaneous Herceptin initiated in patients with early HER2-positive breast
Collaborate with the drug safety team,
for treatment, analysis and the reporting of the adverse drug reactions.
Writing the case reports in the ARISg
safety database, in supporting the SAE reconciliation activities
(interventional and non-interventional studies).
Conduct a drug safety project study to
observe the tolerability of the ACHEI and the Memantine in patients with
October 2014 to
Participate in writing of the case
narratives reports concerning the adverse events occurring in patients during
the study period.
INSERM U894 Academic Center of Research Paris,
in Psychiatry and Neurosciences
Oct 2012 – Oct 2013
-Collaborate and manage different research protocols in the field of the
neurodegenerative pathologies and the memory disorders. My principal
-Collaborate in the project management
-Screen and review of the literature
-Participate in writing the protocol of the research
-Cooperate in the patient’s recruitment, the collection of the clinical data, the
analysis and the interpretation of the
CNRS (UMR 7102)
Jan 2011– Jul 2012
Collaborate in writing research protocol (collection
of the clinical data, the analysis and the interpretation of the results).
2015 to 2017 Master 1 in Pharmacovigilance and
University of Bordeaux.
2014 Professional training in clinical
research (Clinical Research
2011 to 2012 Master 2 in Neurosciences and Neuropsychology.
Marie Curie and Pierre Mendes.
CERTIFICATES AND TRAINING:
2015-2017 Certificate Management Adverse Events (Roche)
11/2017 ICH-GCP (R2)
knowledge of ICH – FDA guidelines.
Literature &Medical writing
management & documentation
&Problem solving skills.
Office and internet application expertise
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