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Looking for a more challenging job opportunity


Current Experience

  • Clinical Trial Assistant (CTA)
    Since January 2015
    ~ Ensure informed consent forms are translated (initial and amendments) ~ Collect necessary documents and compile (as applicable) Ethics Committee submissions (initial and amendments) ~ Collect necessary documents and collate Site Initiation Packages (Investigator Site Files (ISF), Pharmacy binders (IPIM)) ~ Ensure all necessary supplies are on site (e.g. PRO, binders) ~ Communicate with sites regarding trial start-up, conduct, and close-out activities ~ Update databases/systems (eClinical, study specific trackers,…) ~ Archive of essential study documents (TMF – RIM) ~ Provide support to Clinical Operations Management and Clinical Research Associates ~ Work with a variety of teams on several clinical trial projects ~ Implement procedural changes to increase effectiveness and productivity

Past Experience

  • Research Assistant (Internship)
    November 2012 --- June 2014
    Own project: In vitro T-cell differentiation from hESC: a good model for early human T-cell development? I have contributed to the development and delivery of laboratory based research activities. I have worked independently with minimal supervision. Preparing and effectively communicating the laboratory results, methodologies and data to other members of the research group was the most important part of the job. During the project, I have learned to finish work by pre-set deadlines and improved my eye for details. I have suggested research ideas and have actively participated in the planning of the research activities. Furthermore, I maintained a comprehensive and well-documented lab notebook and followed the health and safety regulations and legal requirements. By being a research assistant, I obtained experience in growing and handling of cell cultures, flow cytometry and real time PCR.

  • Ski Instructor
    January 2009 --- January 2013

  • Child animator
    January 2008 --- January 2012


LinkedIn Assessment :
molecular biologyCell biologyBiochemistryscienceResearchLifesciencesGeneticsMicrobiologyMicrosoft ExcelMicrosoft WordPowerPointICH-GCPSOP


  • Level 3 in French from Adult Center for Education, Ghent in 2015
  • Basic ICH GCP Qualification Training Course in Biomedische wetenschappen (Biomedical Sciences) from Universiteit Gent in 2014
  • Master of Science (MS) in Biomedische wetenschappen (Biomedical Sciences) from Universiteit Gent in 2014
  • Bachelor's degree in Biomedische wetenschappen (Biomedical Sciences) from Universiteit Gent in 2012
  • GSE - Science Mathematics in Wetenschappen-Wiskunde from Erasmus Atheneum De Pinte in 2009

Training and Certification

  • Basic ICH GCP Qualification Certification
  • CTA Workshop Certification
  • ICH GCP Qualification Certification
  • Laboratory Animal Sciences Cat. 3 Certification
  • Master’s Degree in Biomedical Sciences Certification

Area / Region

Gent, België


Driving License
  • Yes