
Timeline
About me
sClinical Trial Assistant en Bioclever CRO
Education

Col·legi oficial de metges de barcelona
2013 - 2014Màster en monitorització d' assaigs clínics
Universitat autònoma de barcelona
1997 - 2004Biology biology, general
Universitat autònoma de barcelona
2004 - 2005Prácticas en empresa human/medical genetics departamento de citogenética en el laboratorio balague center
Experience

Balague center
Oct 2004 - Jul 2014Coordinación del departamento de Automáticos, con analizadores bioquímicos de carga contínua.Validación de resultados.Control de resultados pendientes y demoras. Análisis citogenéticos aplicados a muestras de sangre periférica (estudios constitucionales y oncohematológicos), médula ósea (estudios oncohematológicos), líquido amniótico y vellosidades coriales (estudios de Diagnóstico Prenatal).También se ha impartido clases teóricas y prácticas a universitarios que realizaban sus prácticas en esta empresa.
Co-responsable Dpto.Bioquímica Automatizada
Jul 2013 - Jul 2014Citogenetista
Oct 2004 - Jul 2013

Saalig clinical
Mar 2015 - Dec 2015Clinical trial assistantCTA. Gestió administrativa d’ assajos clínics i estudis observacionals. Marc legal. Presentació documentació a CEIC’s i AEMPS. Elaboració i gestió de contractes entre Fund-Promotor-Hospital. Memòria econòmica. Data Entry. Gestió factures. Monitorització a distància. Edició de Protocols. Esmenes i Anexes de contractes. HIP.CI.

Cerba internacional sae
Jan 2016 - Mar 2016Citogenetista
Adknoma health research
Apr 2016 - Nov 2020Cra/cta- Responsible for observational studies submissions. Ensure the success in observational studies in order to obtain the necessary authorizations in line with current legislation and to reach the project objectives.- Submissions to AEMPS and EC (AEMPS, PEIBA).- Responsible during the start-up in the assigned projects.- Contact person with local and national authorities, submissions, regulatory advisor.- Management and negotiation of contracts with sites.- Follow-up communications (FPFV, ASR, LPLV, FR, etc).- Amendments (substantial and non-substantial). - Control of payments of EC fees and invoices for patient recruitment.Phases:Observational, post-marketed studies with medication. Therapeutics areas: Endocrinology, Nephrology, Neurology, EPOC.Observational, pots-marketed studies with medical devices. Therapeutics areas: Gynaecology (Infectious diseases), Rheumatology.Clinical Trial with medication, phase II. Therapeutics areas: critical careClinical Trial with medical devices, phase II. Therapeutics areas: Gynaecology (Infectious diseases). Show less

Bioclever cro
Dec 2020 - nowSclinical trial assistantSenior Start-Up Specialist & CTA
Licenses & Certifications

Ich good clinical practice e6 (r2)
The global health networkDec 2020
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