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Awa NdawAN

Awa Ndaw

Clinical Trial Manager – Freelance

790 €/jour
Paris, FR
15 ans et +

Délai de réponse moyen : 1h

À propos de Awa

Clinical Operations Consultant with 15+ years of experience in international clinical research, particularly in oncology and multicenter Phase I–IV studies.

I support sponsors and CROs with study coordination, operational oversight, CRA management, ICH-GCP compliance, and Clinical Trial Management support activities.

Recognized for my professionalism, strong organizational skills, and ability to collaborate effectively with international teams, I am also appreciated for my communication skills, diplomacy, adaptability, and collaborative mindset.

Autonomous, detail-oriented, and highly committed, I place strong emphasis on quality, communication, and meeting timelines.

Available for remote / home-based freelance assignments in Clinical Operations.
  • Français

    Bilingue ou natif

  • Anglais

    Capacité professionnelle complète

  • Allemand

    Notions

En télétravail uniquement
Travaille majoritairement à distance

Expériences

  • TRIO Oncology,
    Clinical Trial Manager – Freelance
    SECTEUR MÉDICAL
    février 2020 - février 2025 (5 ans)
    France
    • Oversaw country and site activities across Phase I–III oncology studies
    • Supervised CRAs and ensured high-quality monitoring & ICH-GCP compliance
    • Reviewed monitoring reports, deviations and CAPAs
    • Coordinated regulatory submissions across EU & UK
    • Supported TMF quality, inspection readiness, vendor & financial oversight
    Clinical Trial Management GCP Compliance Regulatory Affairs Financial Oversight Inspection Readiness
  • Freelance | TRIO Oncology,
    Senior Clinical Research Associate
    août 2016 - mars 2020 (3 ans et 7 mois)
    France
    • Managed up to 15 sites and 75+ patients in Phase II–III breast cancer studies
    • Conducted monitoring visits, SDV, SAE reporting, and IMP accountability
    • Collaborated with cross-functional teams (PM, DM, PV, QA)
  • Covance
    Senior Clinical Research Associate
    octobre 2014 - juillet 2016 (1 an et 9 mois)
    France
    • Led site monitoring for Phase I–III studies in oncology and neurology
    • Supported study start-up activities and site initiation
    • Ensured protocol compliance and data quality across multiple sites

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Formations

  • Clinical Research Training
    CLINACT INFO
    2010
    Clinical Research Training
  • Master's Degree
    INSEEC Business School
    2009
    Master's Degree

Catégories

  • Autre