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Summary

I'm a consultant in the life sciences industry with experience in clinical research, validation and quality & compliance projects.

Experiences

Current Experience

  • Life Sciences Consultant
    Since August 2013

Past Experience

  • Validation Engineer
    October 2012 --- August 2013

  • ESDS Assistant (Clinical Research)
    December 2011 --- October 2012

  • Pharmaceutical Assistant (interim)
    September 2011 --- December 2011

Knowledge

Self Assessment :
Clinical research Phase I Scientific writingClinical Data Management (CDM)Clinical trialsCTMSData entryElectronic Data Capture (EDC) Good Manufacturing Practice (GMP)ICH GCP guidelinesValidationScientific WritingRegulatory submissions
LinkedIn Assessment :
MatlabEngineeringMicrosoft OfficeExcelWordLife SciencesResearchPowerPointClinical researchQuality Assurance (QA)LifesciencesValidationGMPPharmaceutical Industry

Skills and Expertise

Self Assessment :
Analyze data Control data Interpret data Report dataCoachCollaborate with project teamConduct monitor visitsData validationData verificationManage clinical trial files/documentsManage Clinical Trial Management System (CTMS) lifescienceWriting regulatory documentsSupervise trial suppliesStudy-related documents

Education

  • Master in Bioengineering from University Ghent in 2011

Area / Region

Zele, Belgium

Others

Driving License
  • Yes