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Louise GOEDHART

PARIS

En résumé

Mes compétences :
Osteoporosis
ICH
GCP
Clinical Research
Cardiology
responsible for the commercial development
Public Relations
Provide medical training
Project Management tasks
Project Management
Performing Monitoring
Paediatrics
Oncology
Neurology
Multiple sclerosis
Microsoft Word
Microsoft PowerPoint
Microsoft Outlook
Microsoft Excel
Hypertension
Extensive international experience
Endocrinology
Angina
Account Management
Communication
Industrie pharmaceutique

Entreprises

  • Quintiles Benefit France - Coordinateur de Recherche Clinique

    maintenant
  • Talent & Pro - Project Assistant

    maintenant
  • INC Research - Clinical Team Manager

    2015 - maintenant *Review of monitoring Visit Reports on several studies, Quality Check of Trail Master File, Review of INR trackers,
    Provide eCRF Trainings to monitors and medical reviewers both at CRO and Sponsor Level and several other
    coordinating tasks.

    *Collection of essential documents, performing Site Initiation Visits and Clinical Lead tasks on a Phase IIIb,
    multinational, multicenter, open label, randomized withdrawal Pediatrics trial on Hyponatremia.
  • Quintiles Contract Research Organization - Senior Clinical Research Associate/Lead CRA

    2010 - 2015 *Review of monitoring Visit Reports on several studies, Quality Check of Trail Master File, Review of INR trackers,
    Provide eCRF Trainings to monitors and medical reviewers both at CRO and Sponsor Level and several other
    coordinating tasks.

    *Performing Monitoring and Close-Out visits on a Global Phase IIIb trial testing the efficacy and safety of a CETPinhibitor in patients with Acute Coronary Syndrome. Approximately 15.600 enrolled patients worldwide. Study
    duration 5 years.

    *Data Cleaning and Close-Out Visits on a Global study to assess the safety and efficacy of a novel oral anticoagulant
    versus standard practice of dosing with Warfarin in patients with Atrial Fibrillation. More than 21.000 patients
    enrolled worldwide. Study duration 5 years.

    *Site Initiation, Monitoring, Close-Out Visits, Monitoring Report Review and Coordinating Tasks on multiple Phase IV
    interventional and observational studies testing the safety and efficacy of several drugs in Multiple Sclerosis.

    *Site Initiation and Monitoring Visits on a Multinational Phase III trial evaluating the safety and efficacy of a MEKinhibitor on patients with Uveal Melanoma.


    Medical Respresentative
  • Laboratoires Servier - Medical Representative

    2007 - 2009
  • Servier Pharmaceutical Company - Medical Representative

    2007 - 2009 * Commercial development of several drugs in osteoporosis, hypertension and angina pectoris ;
    * Editing daily and monthly Sales Reports
    * Organisation of Medical Events
    * Editing Commercial Action Plans
    * Provide medical training to doctors
  • Talent & Pro - Project Assistant

    2005 - 2006

Formations

  • NEOMA BUSINESS SCHOOL

    Paris 2015 - maintenant Executive MBA

    NEOMA Business School's EQUIS, AACSB and AMBA triple-crown accreditation status makes it one of the few French institutions of its kind to fully meet international academic standards. Professors are leading teacher-researchers with prior experience in some of the world's most reputated schools and universities.

    The shool conducts in-depth, business-relevant research that meets the very highest
  • Insitut Léonard De Vinci

    Paris La Défense 2009 - 2010 Executive Master

    Certification in Clinical Research
  • University Of Amsterdam (Amsterdam)

    Amsterdam 2000 - 2004 Master of Arts

    French Literature, Language and Culture
  • University Of Amsterdam (Amsterdam)

    Amsterdam 1999 - 2004 Bachelor Economic Sciences
  • Hogeschool Schoevers (Amsterdam)

    Amsterdam 1998 - 1999 Account Management/Public Relations

Réseau

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