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Awa NdawAN

Average response time: 1 hour

About 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.
  • French

    Native or bilingual

  • English

    Fluent

  • German

    Basic

Remote only
Primarily works remotely

Experience

  • TRIO Oncology,
    Clinical Trial Manager – Freelance
    MEDICAL
    February 2020 - February 2025 (5 years)
    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
    August 2016 - March 2020 (3 years and 7 months)
    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
    October 2014 - July 2016 (1 year and 9 months)
    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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Education

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

Categories

  • Other