About the specialist
Graduated with a Master’s degree in Chemistry from the University of Warsaw. In 2023, completed postgraduate studies in Master of Business Administration – Clinical Trials in Warsaw, gaining comprehensive training in conducting and coordinating clinical trials in compliance with Good Clinical Practice (GCP) guidelines and current legal regulations. The program combined scientific, legal, and managerial topics, focusing on effective planning of research projects, implementing innovative therapies, and registration procedures for drugs and medical devices.
In 2022, joined the Clinical Trials Team as a Coordinator. Responsible for organizing and overseeing the progress of trials, ensuring compliance with protocols, legal regulations, and the highest ethical standards. Collaborates with researchers, sponsors, and CROs, coordinating patient visits and maintaining trial documentation. Supports the recruitment of trial participants, monitors the execution of procedures according to the schedule, and prepares the site for audits and inspections, ensuring the highest quality of the projects conducted.
Holds a valid Good Clinical Practice (GCP) certification. A member of the Association for Good Clinical Practice in Poland (GCPpl), regularly participating in courses, training sessions, and industry events, both online and in person. Actively engages in conferences focused on clinical trials, keeping up with the latest trends, regulatory changes, and innovative approaches to conducting research. Regularly participates in training sessions organized by the Medical Research Agency, staying updated on the latest regulations, research methodologies, and best practices in managing research processes. Actively involved in initiatives aimed at improving the quality and efficiency of research conducted in Poland, supporting the development and implementation of best practices in the field of research on new therapies.