Cecilia Oria

Responsible, dynamic and proactive professional, with ease of adaptation and organization. I have knowledge about control systems, quality and integrity of data according to global GCP in Clinical Research, notions about regulatory affairs, Quick adaptability for handling computer programs and ability to work in a team under high pressure conditions. Persevering and eager to work and continue learning; focused on solving problems efficiently in order to achieve the goals set by the company.

Professional with more than 4 years of experience in Clinical Research working as a Data Manager and lately as a Clinical Research Study Coordinator, with great knowledge about start - up management of clinical trials, ethics and regulatory submites, general coordination activities, data integrity, quality, control system operations, and maintenance of confidential documentation in accordance with clinical research regulatory requirements (Good Clinical Practices - GCP, Guidelines of the International Conference on Harmonization (ICH), Bioethics, basic notions on Regulatory Affairs, etc) and SOP to evaluate the safety and efficacy of the products under Investigation for the site, during the initiation, the development of the protocol and the closing.

In addition, I have extensive computer software experience, with a quick learning of new software and excellent organization, record keeping and time management skills. Persevering and eager to work and continue learning; focused on solving problems efficiently in order to achieve the goals set by the company.

MASTER IN CLINICAL RESEARCH 03/2022 - 12/2022

San Martin de Porres University - USMP. (Graduated)

Víctor Alzamora Castro Graduate School. Peruvian University Cayetano Heredia