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Valérie MOUTON COSSON

Slough

Electionseuropéennes 2024

RETROUVEZ GRATUITEMENTLe résultat des européennes au Mans ainsi que le résultat des européennes dans la Sarthe.

En résumé

I am a CRA with 6 years of experience in international clinical trials, Phase I to III, in Oncology (Haematology Oncology) and Haematology.
Thanks to my 25-year experience in pharmaceutical industry, I have a broad knowledge in various therapeutic areas: oncology (pneumology, breast cancer, prostate, lymphoma and leukemia) and neurology, dermatology, pneumology, gynecology, gastroenterology, nephrology and cardiology.

Mes compétences :
Santé
Industrie pharmaceutique
Communication
Management
Pharmacie
Formation
Informatique

Entreprises

  • Chiltern International - Clinical Research Associate II / Oncology Haematology

    Slough 2015 - maintenant Therapeutic Area/ Indication/ Lab Experience
    • Onco-Hematology

    Key areas of Responsibility:
    • Monitor oncology clinical trials phase I to III
    • Prepare and conduct all kind of on-site visits according to relevant SOPs and document
    them (visit report and follow-up letter).
    • Review the signed informed consents
    • Conduct source data verification and CRF discrepancy resolution
    • Provide information about patient recruitment, site status, SAE status, protocol
    deviations and any other important information to the project team regarding my own
    sites.
    • Ensure all the serious adverse events have been appropriately reported.
    Follow-up of drug safety issues and safety reports in timely manners, if applicable.
    • Collect essential documents and any updates on an ongoing basis, and ensure that
    investigator and pharmacy site files are up to date.
    • Ensure that all study related communication including e-mail is filed on site and in the
    sponsor files.
    • To ensure that sites have sufficient supplies (study drug, central lab kits …).
    • Ensure proper storage, dispensation and accountability of the study drug.
    • Prepare and follow investigator payments.
    • Communicate site study issues, concerns, and progress to Project Manager, Clinical
    Team Lead and Clinical Research Manager accordingly

  • RPS / PRA for Celgene - Oncology Clinical Research Associate I

    2012 - 2015

  • Celgene - Oncology Clinical Research Associate

    Paris 2011 - 2011

  • Genzyme - Responsable Regionale

    Saint-Germain-en-Laye 2008 - 2010

  • Topotarget - Responsable Grands Comptes

    2006 - 2008

  • Amgen SAS - Attachée Scientifique Hospitalière

    PARIS 2001 - 2006

  • FERRING - Déléguée Médicale Spécialiste

    1991 - 2001

Formations

Réseau

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