Karolina Chrystow-Chrystow is a professional in the clinical research field with experience spanning multiple roles in prominent organizations. Beginning as a Clinical Trial Assistant at IQ Pharma S.A., responsibilities included managing documents for regulatory offices, coordinating communication with vendors and CRAs, and preparing trial master files. Progressing to roles such as Project Manager and Pharmacovigilance Specialist, Karolina oversaw clinical trials and managed safety reporting within Eudravigilance. After continuing growth at IQVIA and TFS - Clinical Contract Research Organization, Karolina advanced to Senior Clinical Research Associate I. Karolina holds a Master of Pharmacy from ÅšlÄ…ski Uniwersytet Medyczny and a postgraduate degree in Conducting and Monitoring Clinical Trials from Kozminski University.
Location
Warsaw, Poland
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