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Rida ATMI is an experienced professional in clinical quality assurance and regulatory affairs, currently serving as a Clinical Quality Assurance Associate at Unicancer since April 2008. Responsibilities include implementing quality management systems in line with GCP, conducting audits, managing non-conformities and CAPA, and providing employee training. Previously, Rida held the position of Regulatory Affairs Associate Senior, focusing on the submission of clinical trial applications, substantial modifications, and incident management. Prior experience includes serving as a Clinical Trial Assessor at ANSM, where assessments of viral safety records were performed, and a Laboratory Technician at Institut Curie, specializing in recombinant protein processes. Rida holds a D.U in quality assurance and risk management from Université de Tours, a Master’s in industrial genomics from École de Biologie Industrielle, and further education in molecular biology and drug development.