Iñaki Díaz Junguitu Fernández I am a biochemist by training, having completed my degree at the University of Navarra and a master’s degree in Clinical Research Applied to Oncology. I currently work at the Support Unit for Ethics Committees (USCE), where I specialize in the legal framework and authorization process for different types of clinical research, focusing primarily on clinical trials. My professional journey has allowed me to develop great versatility and proactivity in managing clinical research, as well as in course coordination and teaching. I am also the coordinator of the CTA course and a professor in the Master’s in Clinical Trials Management and Coordination. My goal is to ensure that research processes meet ethical and legal standards, thus contributing to the advancement of science in a responsible and effective manner. Instituciones de las que forman parte PGestio i Adm. Cap unitat Unidad de Apoyo a los Comités de Ética (USCE) Dirección de Estrategia Externa Vall Hebron Institut de Recerca LinkedIn Twitter Iñaki Díaz Junguitu Fernández LinkedIn Twitter Instituciones de las que forman parte PGestio i Adm. Cap unitat Unidad de Apoyo a los Comités de Ética (USCE) Dirección de Estrategia Externa Vall Hebron Institut de Recerca I am a biochemist by training, having completed my degree at the University of Navarra and a master’s degree in Clinical Research Applied to Oncology. I currently work at the Support Unit for Ethics Committees (USCE), where I specialize in the legal framework and authorization process for different types of clinical research, focusing primarily on clinical trials. My professional journey has allowed me to develop great versatility and proactivity in managing clinical research, as well as in course coordination and teaching. I am also the coordinator of the CTA course and a professor in the Master’s in Clinical Trials Management and Coordination. My goal is to ensure that research processes meet ethical and legal standards, thus contributing to the advancement of science in a responsible and effective manner.
Project Manager CEIm Vall d’Hebron Institute of Research (VHIR) January 2020 – Present Supervisor and teacher of the CTA course. Internal trainer in the new European regulation and CTIS. Follow-up coordinator and manager of Clinical Trials. Member of the AEMPS-CEIms Coordination Group. CEIm–Promoters and CEIm–AEMPS communication link. Processing of amendments and clarifications of clinical trials. Clinical Trial Assistant TFS CRO May 2019 – November 2019 eCRF data entry. National submission. ICF editing. Clinical Study Coordinator – Intern HM Hospitales April 2018 – June 2018 Internship as coordinator and data entry in phase II and III oncology clinical trials. R&D Intern PharmaMar November 2017 – March 2018 Mechanism of Action department: cell cultures, RIME, data analysis, immunohistochemistry. Master’s thesis entitled: “Search for the mechanism of action of an antitumor drug through a RIME assay.”
