Digitalization in Clinical Trials MasterClass - EU edition

Through more than 20 years of experience with high-ranking, international pharmaceutical and biotechnological companies as well as Contract Research Organizations Karin has acquired proven expertise in the field of clinical research and compliance with high quality standards. As a trained biologist with a PhD in cancer research Karin started her career in clinical research as a Freelance CRA. Soon thereafter she joined one of the major globally acting pharmaceutical companies as Clinical Study Manager in various indications and with a passion for quality and training. Due to a very focused and structured work attitude and being able to provide quick decisions and recommendations Karin moved into positions of increased responsibility. Karin successfully supported and prepared sites for audits and inspections and gained extensive European and Global experience by performing sponsor oversight in the indication of Rare Diseases. Having founded her own company in 2019 Karin performs trainings and consults on processes regarding Sponsor Oversight, Risk Management and Clinical Trial Management. As Auditor Karin conducts investigator site audits and vendor audits and supports inspection preparations.