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Summary

In search of a starting opportunity as regulatory affairs office, quality manager, pharmacovigilance officer, data manager. Motivated, punctual and certainly eager to learn more on the job. I would like to join your team and company.

Experiences

Past Experience

  • Master thesis student
    September 2014 --- June 2015

  • Member of the year counsel
    October 2013 --- June 2014
    Organizing after school activities

  • WG PR
    June 2013 --- June 2014
    setting up a sponsor file and collecting information of future possible companies who could be interested in supporting medical students

  • Member of the year counsel
    October 2012 --- June 2013
    organizing after school activities

Personality

BrightOwl Assessment :
Anger commandPerspectiveInterest in knowledgeDependability
Self Assessment :
CollaborationCoordinationCritical thinkingKindnessWillingness to compromiseTrustCommunicativeService orientedAttention to detailResponsibilityAdaptabilityCreative thinkingInterest in knowledgeProblem solvingIndependence

Knowledge

BrightOwl Assessment :
MicrobiologySerious Adverse Event (SAE)Data AnalysisPharmacovigilanceDrug regulatory authoritiesRegulatory RequirementsUnderstanding of regulatory guidelinesPatentsDrug development processUnderstand levels of research evidence
Self Assessment :
Interpret systematic reviewsSearch literature on clinical trialsData Analysis
LinkedIn Assessment :
TeamworkCreativitydutchMicrosoft OfficeEnglishSocial SkillsMouse HandlingFrenchCell CultureqPCRRNA extractionStatisticsGraphPad PrismScientific WritingMicrobiologyDatabasesSystematic ReviewsEvidence-based MedicineMeta-analysisLife SciencesR

Skills and Expertise

BrightOwl Assessment :
Control data Analyze dataCreates a collaborative team environmentmanaging a small team Interpret dataAnalyze data/information to determine potential relationships.Data validationEnsure data consistencyEnsure data integrityVerify dataCapture data on source documentsCollaborate with project team

Education

  • Master in Biomedical Sciences from KU Leuven in 2015
  • Master of Biomedical Sciences in minor Management en communicatie from KU Leuven in 2015
  • Bachelor in Biomedical Sciences from KU Leuven in 2014
  • Bachelor of Biomedical Sciences in from Katholieke Universiteit Leuven in 2014
  • Wetenschappen-Wiskunde in from Pleinschool in 2008

Training and Certification

  • FELASA B in 2013 Certification

Languages

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

Work Preferences

  • Positions I am interested in:
    Drug Safety Officer Pharmacovigilance Assistant Pharmacovigilance Officer Regulatory Affairs Assistant Regulatory Affairs Associate Regulatory Affairs Consultant Regulatory Affairs Officer Junior Scientist Biomedical Scientist Clinical Safety Associate Data Manager Data Reviewer Clinical Data Reviewer Clinical Data Manager (DM) QA Officer
  • Positions I am NOT interested in:
    Clinical Research Associate (CRA)
  • Locations I am interested in:
    Brussels, Belgium East Flanders, Belgium Mechelen, Belgium West Flanders, Belgium
  • Work From Home:
    Yes, 0 to 5 days per week
  • International:
    Yes

Area / Region

Kortrijk, Belgium

Others

Driving License
  • Yes