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Fabrice POLLIER

Dubai

En résumé

With more than 10 years of experience in Clinical Research, I dealt with Drugs, Medical Devices and
Therapeutic Cellular Products, for Multinational Projects.

Mes compétences :
Gestion de projet
Assurance qualité
Activités de monitoring
Gestion des sites cliniques
Conception-rédaction de documents
Affaires réglementaires

Entreprises

  • Iris Pharma - Clinical Project Manager

    Dubai 2016 - maintenant

  • CHU Nice - Moniteur pour un projet onco-hématologie pédiatrique / ARC service infectiologie

    Nice 2015 - 2015

  • CHU Nice - ARC

    Nice 2014 - 2015 ARC hospitalier au sein du service de dermatologie

  • Sofradim Production - Groupe COVIDIEN - Senior CRA

    2010 - 2012 Definition of pre and post-market clinical strategy and study design for medical devices in development for hernia repair.
    Medical Device Clinical Evaluation (Annex X Directive 93/42/CEE and MEDDEV 2.7.1 Rev.3 guidance).
    Operating Clinical Trial management.

  • Galderma - Clinical Projects Manager

    Courbevoie 2008 - 2010 Clinical trials Management from study design to study results presentation to marketing team, for international projects.
    CRO management for monitoring and Data Management activities.
    Budget follow-up.
    Staff objectives definition and appraisals (management of an internal Clinical Trial Administrator).

  • Laboratoires Genévrier - Clinical Projects Manager

    ANTIBES 2002 - 2008 Operating Clinical Trials Management for European Clinical Trials from study design to clinical study report, including monitoring activities.
    Management of internal CRAs.

  • Optimed - Clinical Research Associate

    1999 - 2002 Monitoring of phase II and phase III Clinical Trials.
    Clinical Trials Technician and Quality Assurance for phase I studies.

Formations

Réseau

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