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Experiences

Current Experience

  • Technical Regulatory Affairs Scientist


    Since October 2013

Past Experience

  • PhD student

    October 2011 --- September 2012
    development of tissue-engineered heart muscle based on induced pluripotent Stem Cells for drug screening

  • Trainee

    September 2010 --- May 2011
    developing new drugs for the Treatment of huntington disease and other hyperkinetic disorders

Personality

Self Assessment :
Analytical thinkingAttention to detailCollaborationCritical thinkingEfficiencyIndependenceOptimismProblem solvingWillingness to compromise

Knowledge

Self Assessment :
Regulatory affairsHealth EconomicsQuality Assurance (QA) Scientific writingCMC Knowledge of the drug development processMedical writing
LinkedIn Assessment :
Drug Developmentmolecular biologyCell CultureStem Cells

Skills and Expertise

Self Assessment :
scientific writingCoordinate projectsproject managementCoordinate CMC-activitiesChemistry Manufacturing and Controls (CMC) activitiesManage regulatory activities

Education

  • Master of Science (M.Sc.) in Management from Katholieke Universiteit Leuven in 2012
  • Master of Science (M.Sc.) in Drug Develpment from Katholieke Universiteit Leuven in 2011
  • Bachelor's degree in Pharmaceutical Sciences from Katholieke Universiteit Leuven in 2009
  • in Greek & Sciences from Sint-Albertuscollege College Haasrode in 2006

Languages

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

Work Preferences

  • Locations I am interested in:
    Belgium
  • Work From Home:
    Yes, 0 to 5 days per week
  • International:
    No

Area / Region

Leuven, België

Others

Driving License
  • Yes

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