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Nicolas DAOUT

Durham

En résumé

My online CV: http://www.doyoubuzz.com/daout-nicolas/

16 years experience in clinical research (in a wide range of Therapeutic areas including: Rheumatology, Multiple Sclerosis, Diabetes, Neuropathy and Cardiovascular).
Being a key actor as technician, Clinical Research Associate (in-house and on-site) or line manager in trials from phase I to phase IV.
Today, I'm Global International Clinical Project Manager.

Expertises: finance / budgeting, focused project strategy, project instruction writing, innovating monitoring model, recruitment tools leadership, resourcing / staffing, presentation skills, customer relation, vendor & third parties management, problem solving, IVRS/IWRS, ICH/GCP quality, CRA experience, line management, trainer.

Mes compétences :
presentation skills
trainer
problem solving
finance / budgeting
focused project strategy
project instruction writing
innovating monitoring model
recruitment tools leadership
resourcing / staffing
vendor & third parties management
IVRS/IWRS
ICH/GCP quality
CRA experience
line management

Entreprises

  • QuintilesIMS - Global International Clinical Project Manager

    Durham 2011 - maintenant - Manage and co-ordinate efforts of cross-functional project teams to support milestone achievement and to manage study issues and obstacles and ensure consistent use of study tools and training materials and compliance with standard processes, policies and procedures.
    - Manage and co-ordinate Vendor & Third Parties, System specification & Test versus protocol, project & customer needs,
    - Develop study management plans, together with team assignments and accountabilities and oversight of database maintenance.
    - Serve as primary project contact with Sponsor to ensure communication is maintained and reporting schedules are adhered to.
    - Collect information on team performance against contract, customer expectations, and project baselines.
    - Lead problem solving and resolution efforts to include management of risk, contingencies and issues.
    - Identify quality issues within the study to implement appropriate corrective action plans. Escalate findings and action plans to appropriate parties.
    - Provide input for the development of proposals for new work and manage project budgets.
    - Provide input to line managers of their project team members’ performance relative to project tasks.
    - Prepare and present project information at internal and external meetings.
    - Participate in proposal development and in the bid-defense process with guidance and supervision.
    - Ensure high performance and efficiency of the clinical team through the scheduling of co-monitoring/accompanied site/visits and ongoing mentoring of CRA team.

    III – Diabetes Mellitus Type 2 - 24 countries (US; WE; EE; Asia) - 764 sites / 10.000 pts.
    IV – Rheumatoid Arthritis - 33 countries (US; WE; EE; Asia) - 480 sites / 2.800 pts.
    IIIb - Acute Coronary Syndrome - 22 countries (US; WE; EE; Asia) - 590 sites / 20.000 pts
    IV - Multiple Sclerosis - 16 countries (US; WE; EE) - 300 sites / 5.000 pts
    IV – Epidemiological - 1 country (France) - 3.850 sites / 15.250 pts
  • QuintilesIMS - Line Manager

    Durham 2009 - 2011 - 16 Direct Reports (off-site or face to face),
    - Career Management: Project support; Resourcing; One to one, staff performance review, Interview,
    - Trainer: Inspection Readiness Training; Workshop ICH/GCP; Department Presentation / Development of Inter-Departmental Synergy,
    - Department initiative: Coaching Mentoring Program; WE Resourcing call & Meeting; Business Fundamental knowledge Assessment,
  • QuintilesIMS - Senior on site / in house Clinical Research Associate

    Durham 2006 - 2009 France - Permanent contract - October 2006 → April 2009 (senior position from Oct 2007)
  • ASTER-CEPHAC - Technician & Clinical Research Associate

    2001 - 2006 - Clinical Trial: Phase I (France)
    - CNS - Psychiatry - Pain - Alzheimer
    - Cardiology
    - Internal Medicine - Inflammatory - Infection
    - Internal set-up of phase l study, EC submission (including ICF management), e-CRFs, declaration of intent; Follow-up: Management of recruitment, data quality check, safety reports, samples and source documents; queries and monitoring,
    - Key sponsor contact, close collaboration with investigator, local lab, volunteer recruitment department,
  • PIZZA HUT - Server

    Paris 2001 - 2001
  • INSERM - Trainee

    PARIS 13 1999 - 2000 INSERM, Unité 507 Unit (research molecular and cellular biology):
    Mechanism of the cellular inflammation and adhesion in renal diseases

    Research subject: Study manipulation of signal way outcome to integrines CD11b/CD18 activation.

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