Mes compétences :
Industrie pharmaceutique
Gestion de projet
R&D
Entreprises
Novartis
- Associate Global Trial Director (Study Lead)
RUEIL MALMAISON 2017 - maintenant
Novartis
- Expert Clinical Manager - Oncologie
RUEIL MALMAISON 2015 - 2017
Novartis
- Senior Clinical Manager - Oncologie
RUEIL MALMAISON 2014 - 2015
Novartis Pharma AG
- Senior Clinical Manager - Neuroscience
RUEIL MALMAISON 2012 - 2014
Novartis Pharma AG -Basel, Switzerland
- Clinical Manager (Trainee)
2010 - 2012Responsible for supporting, under the leadership of the Clinical Trial Head (CTH), all aspects of clinical trial(s)(Phase II & III)in the NSO department.
Being involved in these studies give me the opportunity to be involved in many tasks such as:
*Check the accuracy of trial information in all trial databases and tracking *Contribute to ongoing scientific review of the clinical data and support trial data analysis, reporting and publishing.
*Participate in the organization and logistics of various oversights (samples management, budget…).
*Help managing/answering questions related to trial procedures and patients’ eligibility.
*Draft Clinical Trial Team meeting minutes. Participate in International Clinical Team meetings.
*Assist with program level activities (development of clinical sections of regulatory documents like safety updates, narratives, Informed Consent Form…)
ADDS
- Clinical Trial Assistant
2009 - maintenantThe main part of my work was to facilitate the follow-up of organisational process of many studies during the holiday period, to contact the investigators to solve administrative problems.
I was also involved into the preparation of two studies (phase III; observational). I have helped to compile initial study documents for submission to the health authorities and drafting the service-rendering specifications for the printing of a Case Report Form.
Hôpital Henri Mondor- Service Nephrologie
- Clinical Research Assistant - Trainee
2008 - maintenantMy main task was to collect clinical data to fill out Case Report Form for an observational study.
I was also in charge of drafting ongoing trial files to facilitate the follow-up of patients by nurses during the clinical nurse vacancies.
