BrightOwl Loader Loading

Summary

                                                                                                                                                   

Experiences

Past Experience

  • In-house Clinical Research Associate/ Clinical Trial Associate Testelt, Scherpenheuvel-Zichem, Belgium

    April 2015 --- September 2015

  • Clinical Research Associate (CRA) Brussels, Belgium

    June 2014 --- October 2014

    indication: -breast Cancer: phase iiib, belgium, 5 sites                      

                                                                          -mcrc: Phase IV, belgium, 36 sites               

    monitoring activities

  • Clinical Research Associate (CRA)/Study Coordinator Brussels, Belgium

    August 2013 --- March 2014

    indication: viral upper Respiratory tract infections Phase III, belgium   

                 34 sites (general practitioners)

    responsibilities: monitoring and close-out visits   

                                                                  

    • study Coordinator                                                                                                                                                  indication: hemato-oncology: Phase IV, belgium

    responsibilities: filling of crfs

  • Clinical Research Associate(Trainee) Louvain-la-Neuve, Ottignies-Louvain-la-Neuve, Belgium

    February 2013 --- May 2013

    indication: viral upper Respiratory tract infections

    Trainee Clinical Trial Associate role.

    Phase III, belgium, 34 sites (general practitioners)

     

    responsibilities:

    • monitoring activities
    • close-out visits

     

  • Clinical Research Fellow (Trainee) Seneffe, Belgium

    October 2012 --- December 2012

         clinet: Expert in Clinical trials: Training                                                                                                                   

    - Planning and management of a clinical project

    - regulatory aspects in use regarding human Experimentation, Good Clinical Practice  

      and responsibilities of the CRA during his visits to Physician investigators

    - writing of scientific documents related to Clinical trials

    - proficiency in Data Management and in the functions of a Data Manager

    - concepts in Biostatistics for Clinical trials and Pharmaceutical Research

    - acquisition of the basic principles for an understanding of the Pharmacovigilance

    - knowledge and understanding of relationships between Pharmacokinetics and  

      Pharmacodynamics.

     

  • Beauty consultant Brussels, Belgium

    February 2011 --- September 2012
    • demonstration of the products
    • Sales of the products

     

  • Conduct a market study Brussels, Belgium

    September 2010 --- November 2010
    • information retrieval on the Internet and from bookstores
    • development of a thesis

     

     

  • Quality Engineer Mont-Saint-Guibert, Belgium

    August 2007 --- May 2009
    • management of customer Quality Assurance department during the transition period
    • participate in execution and implementation of a process on order returns during the launch of a company: Quality Assurance-products distribution
    • support of the interface between fenwal and the logistic company
    • take part in quality meetings at customer sites
    • coordination of complaint handling related to apheresis Disposables and establishment of a new management process

  • QA Engineer Nivelles, Belgium

    October 1999 --- July 2007

     

Personality

Self Assessment :
AdaptabilityAnalytical thinkingAttention to detailCommunicativeCreative thinkingFlexibilityInterest in knowledgeProblem solvingResult Oriented

Knowledge

Self Assessment :
Medical devices R&DBiological Drug DevelopmentcGMPClinical researchCROCurrent Good Manufacturing Practice (CGMP)Data AnalysisDrug development processEnglishGood Clinical Practice (GCP)GMPKnowledge of the drug development processLogisticsMedical DevicesOncology Clinical ResearchPhase IIIProblem-solving methods and troubleshootingProject CoordinationQuality Assurance (QA)SAP

Skills and Expertise

Self Assessment :
Analytical skills Analyze dataCommunicate effectively on different company levelsCommunicationmanaging a small teamTeaching

Education

  • Bachelor Medical biology in Biomedical Laboratory Techniques from Institut Paul Lambin in 2007

Training and Certification

  • ClinEt:Expert in Clinical Trial in 2012 Training
  • Junior CRA training program in 2007 Training
  • GMP training in 2004 Training
  • Languages

    BrightOwl Assessment:
    Self Assessment:
    French
    Native
    English
    Full Proficiency
    Dutch
    Professional Proficiency
    Spanish
    Elementary Proficiency

Work Preferences

  • Positions I am interested in:
    Clinical Research Associate (CRA) QA Engineer QA Officer
  • Work From Home:
    No
  • Work Regime:
    Permanent position :    80%-100% FTE
    BrightOwl freelancer :    40 Hours per week
    BrightOwl employee :    80%-100% FTE
  • International:
    Yes

Area / Region

Brussels, Belgium

Others

Driving License
  • Yes

Similar Candidates

Other Candidates in Belgium

Other Candidates in Brussels

Other similar Candidates in Brussels

Other Candidates

Most Recent Searches

Most Famous Searches

You might also like