Kirsten Van Camp is an experienced clinical research professional, currently serving as a Clinical Research Specialist at Vitaz since November 2016. Prior to this role, Kirsten worked at Alcon, a Novartis company, as a Clinical Trial Document Management Specialist from February 2016 to November 2016. Additionally, Kirsten has extensive experience at SGS Belgium nv, where positions included Clinical Research Associate, Quality Control Officer, and Data Quality Coordinator from 2011 to February 2016. Earlier, Kirsten was a researcher at the University of Antwerp from February 2007 to August 2011, complemented by educational achievements from the same institution.
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