Mes compétences :
Chef de projet
Clinical Trial
Études cliniques
Manager
Microsoft Project
Pharmacovigilance
Entreprises
PAREXEL International
- Medical Project Manager
Paris2010 - maintenant• Coordination and managemenent of Medical and Safety activities on international multi centre trials including: procedures production, resourcing planning, budget forecast and recognition; client meetings
• Management of Data Monitoring Committees and Clinical Endpoints Committee
PAREXEL International
- Pharmacovigilant - Drug Safety Specialist
Paris2005 - 2009• Plan and schedule activities and deliverables
o Development of Serious Adverse Events (SAE)/ Adverse Drug Reactions (ADRs) management and reporting procedures
o SAE processing and reporting including; regulatory reporting; SAE reconciliation
o Training of CRAs to the safety management
• Medical monitoring support: eCRF and laboratory data review, waivers review and tracking. Set up of a tracking tool associated with these activities.
• Meetings with client
I.N.R.A. - Unité de Virologie et Immunologie Moléculaires
- Chercheur doctorant
2002 - 2005Expertise area: Genetic and diagnostic of Togaviridae
• Research project leading in virology/molecular biology: Genetic and diagnostic of Togaviridae
• Bibliographic and literature follow-up
• Scientific writing and publication: 2 international publications and 2 invention patent applications
