Núria Pérez Picazo I have a degree in Pharmacy from University of Barcelona and I have a "Master in monitoring International Clinical Trials" and a "Postgraduate Degree in Pharmacovigilance". Since March 2014 I have been part of Academic Research Organization (ARO) of VHIR. Initially as CRA and since 2015 as Project Manager From 2008 to 2013 I worked as CRA and Project Manager at Anagram-ESIC Institutions of which they are part Clinical Research Development Directorate Vall Hebron Institut de Recerca Email Núria Pérez Picazo Email Institutions of which they are part Clinical Research Development Directorate Vall Hebron Institut de Recerca I have a degree in Pharmacy from University of Barcelona and I have a "Master in monitoring International Clinical Trials" and a "Postgraduate Degree in Pharmacovigilance". Since March 2014 I have been part of Academic Research Organization (ARO) of VHIR. Initially as CRA and since 2015 as Project Manager From 2008 to 2013 I worked as CRA and Project Manager at Anagram-ESIC
Over 15 years of experience working in clinical research as a Clinical Research Associate/CTM. Clinical Research Therapeutic Areas: - cardiovascular - neurology - hematology - oncology - allergology - dermatology - psychiatry - digestive - Otorhinolaryngology - infectious diseases - neurosurgery and traumatology - rheumatology - endocrinology Key Activities: - Clinical Trials and observational studies start-up. - Supervision and follow up of submissions to Ethics Committees and Competent Authorities; allegations management, amendments and notifications. - Identifying and resolving issues - Pre-study, initiation, monitoring and close out visits: Revision of reports - DSUR and annual follow up reports: writing and revision. - Design, adaptation and revision of protocol, PIS+ICF, CRF, monitoring plan, data validation plan and laboratory manual. - Revision of pharmacovigilance and laboratory manual. - Translation of protocol, PIS+ICF, patient diary and other documents of the trial. - Preparation of presentations for pre-study and initiation visits. - Preparation of presentations for investigator’s meetings. - Newsletters: writing - Management and control of trial medication and investigational products according Drug Management Plan. - Creation of labels for study medication. - Creation of laboratory kits. - Contract negotiation - Hiring of vendors: insurance policy, couriers, CRF, laboratory material etc..
Projects Plataforma ISCIII de soporte para la Investigación Clínica IP: Inmaculada Fuentes Camps Collaborators: Gemma Vona Giralt, Antonio Moreno Galdó, Rafael Simó Canonge, Núria Pérez Picazo, Plataforma ISCIII de soporte para la Investigación Clínica , Ariadna Martín Balcells, Olga Sánchez- Maroto Carrizo, Joan Genescà Ferrer, Paula Isabel Roldan Caballero Funding agency: Instituto de Salud Carlos III Funding: 315150 Reference: PT20/00078 Duration: 01/01/2021 - 31/12/2024 Plataforma d'unitats de recerca clínica i assaigs clínics IP: Inmaculada Fuentes Camps Collaborators: Santiago Pérez Hoyos, Antonio Moreno Galdó, Núria Pérez Picazo, Plataforma d'unitats de recerca clínica i assaigs clínics, Ariadna Martín Balcells, Olga Sánchez- Maroto Carrizo Funding agency: Instituto de Salud Carlos III Funding: 585750 Reference: PT13/0002/0028 Duration: 01/01/2014 - 31/12/2018 Benznidazol and Triazol REsearch group for Nanomedicine and Innovation on Chagas disease (BERENICE) Grant Agreement nº 305937 IP: Israel Molina Romero Collaborators: Maria Luisa Aznar Ruiz de Alegria, Núria Pérez Picazo, Fernando M Salvador Velez, Benznidazol and Triazol REsearch group for Nanomedicine and Innovation on Chagas disease (BERENICE) Grant Agreement nº 305937, Adrián Sánchez Montalvá, Elena Sulleiro Igual, Olga Sánchez- Maroto Carrizo, Esperanza Esteban Serna Funding agency: EUROPEAN COMMISSION Funding: 939958.88 Reference: BERENICE_FP7HEALTH2012 Duration: 01/09/2012 - 31/08/2018
