Sobre Francisco Márquez del Pino:
Having worked for many years in different areas and stages of pharmaceutical development, I decided to focus my career in a field that I consider very interesting and with many possibilities of progression, the monitoring of clinical trials. To this end, I have completed the master's degree in clinical trial monitoring at the COFM to work as a CRA.
I am a very motivated and versatile person able to work both in a team and independently and always looking for new challenges. I also have good interpersonal and communication skills that I have been able to develop throughout my working life.
During my experience as a CRA, I have had the opportunity to gain practical knowledge and monitor phase II and III studies, both in oncology and internal medicine.
Experiencia
After a great experience improving my English language skills in the UK, I had the opportunity to return to Spain and work as a pharmacist in different pharmacies in Andalusia.
In September 2014 I moved to Madrid to study for a Master’s degree in Drug Discovery and Development. Through this studies I got the opportunity to do an internship in the vaccines joint venture Sanofi Pasteur MSD. In that position, I worked in the Medical Information Department and also gave support to the Medical Affairs Department. In February 2015, I started an internship in the Clinical Pharmacology Department of the oncology unit of PharmaMar (Madrid). During that period, I participated in the pharmacokinetic and data analysis for different ongoing clinical trials.
After finishing the internship, in October 2015, I started working as Specialist Technician in Pharmacokinetics and Bioanalysis in the preclinical pharmacology department of PharmaMar (Madrid). In this role I was involved in the preclinical development of drug discovery molecules, being responsible for the pharmacokinetic analysis of preclinical trials and the review of the PK results of non-clinical GLP toxicokinetic studies in the oncology area. I had the opportunity of participating in the IMPD, IND and Investigator’s Brochures writing about certain molecules which went on to be tested in clinical trials. I also participated in the submission of the dossier of Lurbinectedin to the FDA, a new molecule which was approved through a fast-track process for metastatic small cell lung cancer (2020). I started the postgraduate studies on monitoring clinical trials of the COFM in September 2021. I joined Pivotal in January 2022 as CRA Trainee.
Educación
- Licentiate’s Degree in Pharmacy (equivalent to Bachelor + Master; 5 years) (Sep 2006 – Jul 2012)
University of Granada
Granada, Spain - Master’s Degree in Monitoring of Clinical Trials (Sep 2021 – Aug 2022)
Colegio Oficial de Farmacéuticos de Madrid (COFM)
Madrid, Spain - Master’s Degree in Drug Discovery and Development (Oct 2014 – Jul 2015)
Rey Juan Carlos University
Madrid, Spain - Master’s degree in Teaching Secondary Education (May 2018 – Apr 2019)
Valencia International University (VIU)
Valencia, Spain
Profesionales del mismo sector Farmacéutica / Biotecnología que Francisco Márquez del Pino
Profesionales de diferentes sectores cerca de Madrid, Madrid
Otros usuarios que se llaman Francisco
Trabajos cerca de Madrid, Madrid
-
Clinical Research Associate
Encontrado en: Buscojobs ES C2 - hace 1 semana
Alpha Bioresearch Madrid, EspañaResponsable de los centros/investigadores de los estudios asignados hasta el cierre de los mismos.Actuar como intermediario entre el promotor de una investigación, el investigador y las institucionesBuena relación con los centros de investigación para garantizar que cumplen con l ...
-
Clinical Research Associate
Encontrado en: Jobgoal ES C2 - hace 1 día
ALPHA BIORESEARCH Madrid, EspañaResponsable de los centros/investigadores de los estudios asignados hasta el cierre de los mismos. · Actuar como intermediario entre el promotor de una investigación, el investigador y las instituciones · Buena relación con los centros de investigación para garantizar que cumplen ...
-
Clinical Trial Assistant
Encontrado en: Buscojobs ES C2 - hace 1 semana
Alpha Bioresearch Madrid, EspañaResponsable de las actividades regulatorias de puesta en marcha, seguimiento y cierre de los estudios de Alpha Bioresearch asignados. Cumpliendo los parámetros de calidad requeridos.Recabar la información de los requerimientos para obtener las aprobaciones de IRB / EC, y la docum ...