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Pascale DUCLOUX

BRUXELLES

En résumé

Mes compétences :
Clinical research
Project management
Cardiology and rhythmology
MRI: Safety and Compatibility of Medical Devices
Engineer
Medical device

Entreprises

  • iSTAR medical - Clinical Operations Senior Manager

    2020 - maintenant
  • Abbott Laboratories - Senior Manager Clinical Project Manager

    Rungis 2019 - 2020
  • Abbott Laboratories - Manager Clinical Project Management

    Rungis 2018 - 2019
  • Abbott Laboratories - Clinical Manager

    Rungis 2017 - 2018 Manage multiple international post-market studies
    Lead clinical project teams
    Manage CT.gov posting
    Contribute to the development of the study protocol, training plan/requirements and other study related documents
    Ensure project quality
    Engage key opinion leaders and internal senior leadership
    Serve as a mentor to CRAs
    Participate to special projects (task forces...)
    Contribute to the development and execute the publication strategy
    Comply with appropriate regulatory requirements
  • St. Jude Medical - Clinical Manager

    Boulogne-Billancourt 2015 - 2016 Manage multiple international post-market studies
    Lead clinical project teams
    Manage CT.gov posting
    Contribute to the development of the study protocol, training plan/requirements and other study related documents
    Ensure project quality
    Engage key opinion leaders and internal senior leadership
    Serve as a mentor to CRAs
    Participate to special projects (task forces...)
    Contribute to the development and execute the publication strategy
    Comply with appropriate regulatory requirements
  • St. Jude Medical - Associate Clinical Manager

    Boulogne-Billancourt 2013 - 2015 1. Clinical trial management:
    Design, implement and manage international clinical studies (timelines, budget)
    Provide clinical scientific support (training)
    Ensure compliance with appropriate regulatory requirements
    Initiate communication with other departments
    2. Clinical data management:
    Oversee interpretation of clinical results and preparation of study reports, presentations and publications
    Provide oversight and support to investigators for papers and presentations
    Identify and access key opinion leaders
    Interface with regulatory authorities
    3. Personnel management:
    Provide leadership to clinical research staff
    Manage personnel resources to support project activities
    Provide guidance and support to direct report
    Identify and create career growth opportunities for direct report
  • St. Jude Medical - Clinical Project Leader

    Boulogne-Billancourt 2011 - 2013 Manage international clinical studies (timelines, budget)
    Lead and train the project team
    Develop/coordinate project management plan and all project associated documents
    Coordinate administrative activities
    Define requirements and coordinate service providers
    Define requirements for committee membership, investigator and center participation to project
    Coordinate centers selection, nomination and initiation
    Coordinate monitoring activities, timely and quality data collection
    Perform data verification
    Coordinate data analysis
    Plan and support scientific communication
    Coordinate and communicate with investigators/physicians boards
    Ensure compliance with appropriate regulatory requirements
  • Sorin - Clinical Project Manager

    Paris 2010 - 2011 Manage international clinical studies (timelines, budget)
    Write study documents
    Coordinate site selection, qualification and initiation
    Coordinate regulatory submissions and administrative activities
    Coordinate monitoring activities
    Organize training sessions
    Manage steering committee, physicians board and investigator meetings
    Interact with cross-functional team
    Lead the project team
    Ensure compliance with appropriate regulatory requirements
  • Sorin - Clinical Research Engineer

    Paris 2003 - 2010 1. Design and clinical evaluation of new functions in treatment and diagnosis:
    Research new concepts
    Write patents
    Write clinical specifications
    Define and implement preclinical and clinical strategy
    2. Clinical project management:
    Write clinical protocols
    Manage budget and planning
    Coordinate and train the project team
    Provide technical support
    3. Exploitation of technical and clinical data:
    Perform data analysis
    Write clinical reports
    Write scientific publications

Formations

  • Society Of Clinical Research Associates (SOCRA) (Chalfont)

    Chalfont 2015 - 2018 Certified Clinical Research Professional

    Society of Clinical Research Associates (SOCRA)
  • Solvay Business School (Bruxelles)

    Bruxelles 2012 - 2013 Accelerated Management Programme
  • Université Grenoble 1 Joseph Fourier

    St Martin D'Heres 2000 - 2003 Master of Engineering in Health Information Technology

Réseau

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