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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
External Strategy Directorate
Vall Hebron Institut de Recerca

Núria Pérez Picazo

Institutions of which they are part

Tècnic/a Grau Superior
Academic Research Organisation (ARO)
Clinical Core Facilities
External Strategy 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, 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, 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

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