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Current Experience

  • Clinical Research Assistant

    Since September 2014
    provide Clinical support for projects accordeons to covance SOP, ICH guidelines and gcp develop and/or maintain tracking systeem for Clinical projects assist in field monitoring responsibilities as assigned by Supervisor Provide clinical support for projects accordeons to Covance SOP, ICH Guidelines and GCP Develop and/or maintain tracking systeem for clinical projects Assist in field monitoring responsibilities as assigned by supervisor

Past Experience

  • Reseacher

    May 2014 --- September 2014
    managing and setting up a new part of the sensory test Lab. writing out parts of the quality manual and different sorts of procedures ( e.g. SOP's), qa and safety Analysis to get ISO 17025 approved.

  • Mathematics Tutor

    September 2013 --- January 2014
    i wanted to give back to the community and found a great project, tutoring teenagers via the University. during this program, which is rewarding in itself, i’m learning to fine tune my skills as a motivator and Teacher.

  • Study Coordinator / CRA inhouse

    April 2009 --- September 2011
    i was responsible for more than 20 Clinical studies (Phase I – iv), sponsored and non-sponsored (hovon, eortc, bone marrow transplant studies). next to tasks as Data Management, setting up schedules for patients and the Research team, organizing and taking part in meetings (interdepartmental and (inter-)national) such as initiation and closing out visits, writing SOP’s., i informed, instructed, motivated and patients, Nursing staff and Research doctors before, during and after a study. i stimulated, controlled and evaluated the science)" rel="nofollow">Protocol loyalty of the Research team and other involved disciplines such as Pharmacovigilance and submitting and communicating with the Ethics committee. and this whilst keeping within budgetary constraints.

  • Bio-analyst

    October 2008 --- April 2009
    my daily tasks were analyzing animal tissue samples or human serum samples of Phase I to iv studies. the goal was to determine the concentration of drugs with LC-MS.


LinkedIn Assessment :
Meeting PlanningClinical trialsClinical researchClinical Data ManagementPharmacovigilanceCommunicationResearch DevelopmentInformed ConsentOrganizing MeetingsMeeting SchedulingAppointment SchedulingTeamworkIndividual WorkIndependenceISO 17025ResearchQuality Assurance (QA)SOP developmentSensory


  • Master of Science (M.Sc.) in Industrial Engineering: Biochemistry from Universiteit Antwerpen in 2014
  • Bachelor's Degree in Biomedical Technology/Technician from Plantijnhogeschool van de provincie Antwerpen in 2008
  • High School in Pharmaceutical Sciences from Rosenberg S.O. in 2003

Training and Certification

  • ICH-GCP in 2015 Certification


BrightOwl Assessment:
Self Assessment:
Full Proficiency
Professional Proficiency

Work Preferences

  • Notice Period:
    12 weeks
  • Work From Home:
  • Work Regime:
    Permanent position
  • International:

Area / Region

Brussel, België


Driving License
  • No

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