Cecilia Matos-Rosa

Cecilia Matos-Rosa, CCRP, RQAP-GCP has over two decades of experience in the field of clinical quality assurance. Cecilia currently serves as the Associate Director of Quality Assurance - GCP at Tonix Pharmaceuticals, where they are responsible for ensuring compliance with regulatory guidelines. Prior to this role, Cecilia worked as the Senior Manager of Clinical Quality Assurance at Intellia Therapeutics, Inc. for two years. Cecilia also held the position of Senior GCP Quality Assurance Manager at Agenus for three years. Cecilia'sextensive experience also includes managerial roles at ARIAD Pharmaceuticls, Inc., where they oversaw the GCP Quality group, and AMAG Pharmaceuticals, Inc., where they managed the CQA GCP Auditing program. Cecilia's expertise expands beyond pharmaceutical companies, as they have worked as a Consultant in global GCP/GLP auditing at CMR & Associates. Cecilia has also worked at various organizations such as Technical Resources International (TRI), DynPort Vaccine Company LLC, A CSC Company, Sigma-tau, and TherImmune, gaining valuable experience in auditing, project management, and regulatory compliance.

Cecilia Matos-Rosa, CCRP, RQAP-GCP, completed their education at the University of Maryland Global Campus in 2009, although the specific degree and field of study are not provided. In 1981, they earned a degree in Technical Administration from Escola Tecnica Duque de Braganca, specializing in Business Administration and Management. Additionally, they obtained the RQAP-GCP certification from the Society of Quality Assurance in April 2017. Furthermore, they have acquired various additional certifications such as Project Leadership, Quality Management Foundations, and The Eight Essential People Skills for Project Management, all from LinkedIn.