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Thierry FERREIRA

PUGET SUR ARGENS

En résumé

As a senior Project Manager, I have managed many phase 1 to 4 international clinical studies in various therapeutics area and at every stage of a project, from feasibility to CSR. I have also participated in several clinical development programs in both Pharma companies and CROs.
I am professional, outgoing, independent, problem resolution-oriented and an excellent communicator. I strongly believe in teamwork and my personality will enable me to fit into your team quickly, making our future collaboration efficient.

Skills:
Project management
Line management
Management of large clinical international studies according to ICH-GCP, FDA regulations & other regulatory requirements
Global team leader
Budget, timeline, risk & quality management
Study set up - EC submissions - Investigator's meetings
Study monitoring - Management of CRA/LCRA teams
Patient recruitment
Vendor management
Regulatory inspections

Mes compétences :
Biotechnology
Line management
Gestion de projet
Recherche médicale clinique
Industrie pharmaceutique

Entreprises

  • Sociéte européene de cardiologie - Head of Department Eurobservational Research programme

    2013 - 2017 Head of the Observational Research department at the ESC. A department of 14 people running non-interventional clinical studies across the globe.

  • Clinical Research Specialist - Freelance

    2012 - maintenant

  • Covance - Senior Project Manager

    Princeton 2011 - 2012 Management of global phase III & IV studies in kidney transplant in paediatric population and in asthma.

    Main point of contact with Sponsor – Responsible for overall client satisfaction – Successful participation in bid defence meetings

  • NicOx - Sr. Clinical Project Manager

    Valbonne 2007 - 2010 Responsible for budget, timelines and quality of clinical trials
    Management of phase 1 (PK/PD) and international phase 3 studies (global studies)
    Close involvement in daily clinical operations (from study design to CSR writing)
    Management of CROs
    Active participation in SOP and internal process improvement.

  • TxCell - Clinical Project Manager

    Valbonne 2006 - 2007 Participation in the development strategy of an auloguous cell therapy technology with particular emphasis on clinical development possibilities.

    Set up of a FIM study in Crohn's disease.

    Development of in-house regulatory knowledge in Clinical Trial Applications for cell therapies, Orphan Designations and clinical development of paediatric drugs.

  • Allergan - Clinical Project Manager

    Courbevoie 2000 - 2005 Responsible for budget, timelines and quality of clinical trials
    Management of phase 1 to 3 studies (global studies) in ophthalmology
    Central point of contact for project team members
    Management of CROs
    Line management of CRAs and of clinical team members
    Acted as mentor to more junior staff
    Participation in process improvement.

Formations

Pas de formation renseignée

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