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 Tècnic/a Grau Superior Academic Research Organisation (ARO) Clinical Core Facilities Core Facilities Area Vall Hebron Institut de Recerca Email Núria Pérez Picazo Email Institutions of which they are part Tècnic/a Grau Superior Academic Research Organisation (ARO) Clinical Core Facilities Core Facilities Area 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, Tamara Del Rio Higueras, Ariadna Martín Balcells, Olga Sánchez- Maroto Carrizo, Angelica Valderrama Rodríguez, 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, Xavier Vidal Guitart, Núria Pérez Picazo, Tamara Del Rio Higueras, Ariadna Martín Balcells, Olga Sánchez- Maroto Carrizo, Angelica Valderrama Rodríguez 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, Tamara Del Rio Higueras, Adrián Sánchez Montalvá, Elena Sulleiro Igual, Olga Sánchez- Maroto Carrizo, Janna Anthonina Slabbekoorn, Esperanza Esteban Serna Funding agency: EUROPEAN COMMISSION Funding: 939958.88 Reference: BERENICE_FP7HEALTH2012 Duration: 01/09/2012 - 31/08/2018
