Bio
Her main task is to coordinate and conduct feasibility assessments of clinical trials. She is also responsible for preparing clinical trial offers and helps with the design and scientific coordination of performance studies and clinical trials conducted in accordance with the principles of Good Clinical Practice (GCP) and relevant standards and guidelines. It is also responsible for support in preparing the initial budget of a clinical trial, as well as contact and cooperation with clinical trial sponsors, as well as contact and cooperation with the company’s foreign branches.