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Experiences

Current Experience

  • Clinical Research Associate (CRA)


    Since February 2014

Past Experience

  • Senior Clinical Research Associate

    May 2011 --- December 2013
    - implements and monitors Clinical trials to ensure sponsor and Investigator obligations are being met and are compliant with applicable local regulatory requirements and ICH guidelines. - performs investigative site file reconciliation; requests any new or updated site-related essential and non-essential documents and reviews them for content, consistency with other documents, and Compliance with appropriate local regulatory requirements, ICH guidelines, project standard operating procedures (sops), and sponsor requirements. - may serve as a resource for and interact with other functional areas to resolve site issues and facilitate project timelines

  • Clinical Research Associate (CRA)

    March 2008 --- May 2011

  • Clinical Trial Specialist

    December 2006 --- March 2008
    conducts and facilitates the study specific start-up activities including selection and regulatory document collection; supports regulatory submissions, in-and external regulatory consultancy, performs ec submissions, Informed Consent customization and contract preparation.

  • International Regulatory Affairs Officer

    February 2005 --- December 2006
    prepared and submitted registrations and variations file to international competent authorities in accordance with local regulations for hormonal medicinal products in the Therapeutic Areas of Gynecology, fertility & obstetrics, men’s Health.

Education

  • Master and 3d cycle in Biomedical Sciences, General from Université de Liège in 2002
  • in from ILM in 0000
  • in from Saint Jean Marie in 0000
  • in from Saint Jean Marie in 0000
  • in from Saint Jean Marie in 0000

Area / Region

Braine le Château

Others

Driving License
  • No

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