Experience

Clinical Trials Team

• Spain
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• • 2016 - Present

• • Aug 2016 - Present

  Clinical Trials Team is a company based in Madrid (Spain) that offers different services in the clinical research field (clinical monitoring, investigator recruitment, CRA and CTA staffing, etc.). Our team is fully committed to our clients, adapting to their circumstances, and focused on delivering high quality results with a cost-effective approach.



inVentiv Health Clinical

• United States
• Pharmaceutical Manufacturing
• 500 - 600 Employee

• Freelance Senior CRA

  • Feb 2016 - Jul 2017

  Senior CRA for Pfizer studies of breast, ovarian and lung cancer of Phase I/II; and for pediatric thromboembolism Phase II studies. Monitoring activities in Spain: -On site monitoring -Site initiation visit -Electronic Trial Master File and Investigator File updating -Verification of subject safety and site adherence to FDA and ICH regulations / guidelines -Review of CRF and Informed Consent Forms -Queries management and resolution -Work with different vendors: Covance, Cogstate, Bioclinica, Perceptive Show less



Cancer Trials Ireland

• Ireland
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Senior CRA

  • Aug 2015 - Jan 2016

  CRA for Pfizer studies of Breast Cancer: - Work with TRIO (Translational Research in Oncology) - Phase II and Phase III studies - Monitoring activities in several sites in Ireland CRA for Pfizer studies of Breast Cancer: - Work with TRIO (Translational Research in Oncology) - Phase II and Phase III studies - Monitoring activities in several sites in Ireland



Parexel

• United States
• Pharmaceutical Manufacturing
• 700 & Above Employee

• SrCRA

  • Feb 2011 - Jul 2015

  Senior CRA for GlaxoSmithKline studies of HIV- Phase II/III, Flu-Phase II, COPD-Phase IV and Benign prostatic hyperplasia-Phase IV. Monitoring Activities in Spain: -On Site monitoring -Site initiation and close out visit -Electronic Trial Master File and Investigator File updating -Verification of subject safety and site adherence to FDA and ICH regulations / guidelines. -Preparation of site for Audit -Review of CRF and Informed Consent Forms -Queries management and resolution -Work with different vendors: Quest Diagnostics, Inform EDC and IRT, Perceptive Show less



GSK

• United Kingdom
• Pharmaceutical Manufacturing
• 700 & Above Employee

• CRA Trainee en GSK

  • Nov 2010 - Feb 2011



APICES

• Spain
• Biotechnology Research
• 1 - 100 Employee

• CRA Trainee

  • Jun 2010 - Oct 2010



Hospital Ramón y Cajal

• Research
• 500 - 600 Employee

• Trainee

  • Mar 2010 - May 2010

  Work at hospital's Ethics Committee Work at hospital's Ethics Committee



Pharmacy

• Madrid y alrededores, España

• Pharmacy Assistant

  • Jul 2004 - Feb 2009

  Pharmacy Assistant in several pharmacies in Madrid in different periods between 2004 and 2009, while studying Pharmacy at university. Pharmacy Assistant in several pharmacies in Madrid in different periods between 2004 and 2009, while studying Pharmacy at university.