Madrid Area, Spain
Clinical Research Associate
Pharmaceuticals
Education
CESIF 2013 — 2013
Project Management in Clinical Research, Clinical research
CELGENE, S.L. 2012 — 2012
Post Authorization Studies
University of Valladolid 2012 — 2012
Drug safety
San Pablo CEU University in collaboration with Madrid Norte Hospital 2010 — 2010
Specialization course in Oncology Trials Monitoring.
University Autonoma of Madrid (Hospital de la Princesa. Madrid) 2009 — 2010
2010. Master, Clinical Trials Monitoring
University if Salamanca 2001 — 2003
Bachelor degree, Biochemistry
University of Salamanca 1996 — 2001
Bachelor degree, Organic Chemistry
Experience
CRO January 2010 - December 2013
Normon Laboratories September 2006 - January 2010
Chemical Iberica, S.L. May 2005 - May 2006
Skills
Oncología, Drug Safety, Laboratorio, Scientific Writing, Clinical Trials, Ciencias naturales, Industria farmacéutica, Investigación clínica, Cromatografía líquida..., Biotecnología, Medical Writing, Validación, Farmacovigilancia, Medical Terminology, eCRF, ICH-GCP, Medical Records, Normas ICH de buenas..., Redacción de textos..., Clinical Monitoring, Ensayos clínicos, Protocolo, Desarrollo clínico, POE, Control clínico, Data Analysis