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Stéphanie NARDELLA

PARIS

En résumé

10 years experience in Clinical Research
International Coordination, management of international projects (4 years),
Monitoring (6 years)
Pharmaceuticals industries, CRO and hospital
Phases I, II, III adults and pediatrics trials
Therapeutic areas: 10 years in Oncology, 3 years in Cardiology and 2 years in Pneumology
Strong knowledge of Clinical Research Regulatory requirements, GCP and ICH guidelines

Entreprises

  • INC Research - International Project Manager in Oncology

    2010 - maintenant

  • Pierre Fabre (Boulogne 92) - International Clinical Study Coordinator in Oncology

    2008 - 2009 Coordination of an international Phase II trial in metastatic Breast Cancer
    Coordination of a national Phase I trial in solid tumors
    Set up of a national Phase I trial in onco-hematology with implementation of a biomarker test

  • Roche (Neuilly-sur-Seine 92) - Senior Clinical Research Associate / Coordinator in Oncology

    2007 - 2008 Coordination of an international Phase III trial in Lymphoma outsourced by a French CRO
    Monitoring of 4 internationals Phases II and III trials in Breast Cancer and Colorectal Cancer

  • Covance (Rueil- Malmaison 92) - Clinical Research Associate

    2002 - 2007 Coordination of an international Phase III trial in advanced Renal Cell Carcinoma
    Monitoring of internationals Phases I, II and III trials in cardiology, in oncology and in pneumology

  • Institut Gustave Roussy (Villejuif 94) - Hospital Clinical Research Associate

    2001 - 2002 Management of internationals Phases I, II and III trials in Renal Cell Carcinoma

  • Rhône Poulenc Rorer (Champagne-Ardennes) - Medical Representative in Cardiology

    1998 - 2001

Formations

Réseau

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