Clinical trials are a fundamental part of the progress of science as they provide a great service in the research of diseases and the development of new treatments. Therefore, I am very interested in contributing as Clinical data entry/Study coordinator within the EECC.I am currently working as a Study Researcher at the Institute of Biomedicine in Seville (IBiS) immersed in the study of hepatocarcinoma.Graduated in Biotechnology (University of Cadiz) with a Master in biomedical research (University of Seville) oriented to the branch of oncology/hematology, my experience has provided me with the following skills and abilities useful for the position Clinical Research Associate/Study coordinator (ENTRY LEVEL):-Knowledge of ICON SOPs, ICH GCP guidelines, appropriate regulations, ICON systems.-Ability to interact with the whole clinical team (CRAs, Safety, Biostatisticians, etc.). -Ability and willingness to travel when required.-Experience in working autonomously, with a sense of urgency and limited supervision.-Ability to work to tight operational deadlines and manage conflicting priorities, good team working skills, good problem solving skills with initiative and enthusiasm to learn.-Strong computer skills, including but not limited to knowledge of a Clinical Trials Management System (CTMS), Electronic Document Management System (EDMS) and MS-Office products such as Excel and Word.-Effective interpersonal skills and good communication, verbal, written and listening skills. Willingness to learn new things and teach others. Administrative organisation (such as being able to properly organise/save emails, etc.).