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Aurélie ROUX

BALTIMORE

En résumé

Pharmacien industriel spécialisé en contrôle qualité et développement analytique, titulaire d'un doctorat (PhD) en chimie analytique, je travaille actuellement pour l'institut national de la santé américain à Baltimore (Maryland, USA).

Retrouvez mon profil plus complet sur LinkedIn
http://www.linkedin.com/pub/roux-aurelie/35/735/b7b
http://www.researchgate.net/profile/Aurelie_Roux/

Mes compétences :
Analytical Chemistry
Biochemistry
Chemistry
Chromatography
HPLC
Life sciences
Mass Spectrometry
Pharmaceuticals
Research
Statistics

Entreprises

  • US National Institutes of Health (NIH) - Postdoctoral Fellow

    2012 - maintenant National Institute on Drug Abuse (NIDA)
    Intramural Research Program (IRP)
    Integrative Neuroscience Research Branch
    Structural Biology Unit (Supervisor: Amina S. Woods)

  • Ecole Centrale Paris (ECP) - Temporary lecturer (Vacataire), Biology Teaching

    2011 - 2011

  • Commissariat à l'Energie Atomique et aux Energies Alternatives (CEA) - Ph.D Student

    2008 - 2011 CEA Saclay
    DVS/ iBiTec-S/ SPI/ LEMM
    Pharmacology and Immunology Service
    Drug metabolism research laboratory (Supervisor: Christophe JUNOT)
    Preparation of PhD in analytical Chemistry. Thesis obtained October 21, 2011.

    Metabolome analysis by liquid chromatography hyphenated to mass-spectrometry: Application to the discovery of new biomarkers for toxic exposure and pathologies.
    Activities: Metabolome analysis, Liquid Chromatography and Mass Spectrometry, Data processing, Chemometrics, Writting of scientific articles, Good Laboratory Practice.

  • Laboratoire de Chimie Structurale Organique et Biologique (LCSOB) - M.Sc training 2

    2008 - 2008 Training period for Master’s degree in analytical chemistry at the Structural organic and biological chemistry laboratory (Supervisor: Jean-Claude TABET)
    Activities: Analysis of non-covalent complexes between peptides and sugars by ESI mass spectrometry.

  • Glaxosmithkline, QC Analytical Process - Pharm.D Training

    2007 - 2007 Training period for the end of pharmaceutical studies and Master’s degree in quality control and analytical development at Glaxosmithkline, QC Analytical Process (Supervisor: Loic PERON)
    Activities: Creation and setting up of a analytical troubleshootings database for production and quality control support.

  • Laboratoires CDM LAVOISIER - Research Scientist

    PARIS 8 2006 - 2006 «Chaix et Du Marais» pharmaceutical laboratory (C.D.M. Lavoisier)
    Activities: Analytical development, stability studies and impurities search by HPLC-UV.

  • Assistance publique - Hôpitaux de Paris (AP-HP) - Pharm.D Training

    Paris 2005 - 2006 Training period in Saint Antoine Hospital.
    Activities:
    - Development and validation of HPLC-UV methods for the control of hospital preparations with narcotic drugs.
    - Pharmaceuticals activities in infectious disease and rheumatology medical services (control of medical prescriptions, interactions and dosage…)

  • Laboratoire de Pharmacochimie Moléculaire et Structurale - M.Sc training 1

    2003 - 2003 Training period for pharmaceuticals studies at Molecular and Structural Pharmacochemistry Laboratory (INSERM U266).
    Activities: Synthesis and structural analysis of new inhibitors of Aminopeptidase A

Formations

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