Holds a Master degree in biochemistry from the Univerté du Québec à Montréal and is responsible for the clinical research operations. He has cumulated over 18 years of experience in clinical research working for university hospital, clinical research organizations (CRO) and pharmaceutical company. Marc managed multiple clinical trials across different therapeutic areas, ensuring compliance with Good Clinical Practice (GCP) and regulatory standards. He has overseen clinical trials from different phases from feasibility, start-up, site selection, maintenance to site close-out. He contributed to the development and implementation of novel and efficient processes and tools to enhance the performance and quality of clinical studies, such as digital solutions, risk-based monitoring, and adaptive design. Marc is driven by the mission of improving the lives of patients and advancing the science of medicine.
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