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Master of Continuing Education in Clinical Trials Monitoring and Pharmaceutical Development

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About this course

This Master in Clinical Trial Monitoring and Pharmaceutical Development is aimed at those who have a university degree in health sciences, either pharmacy, medicine, chemistry, biology, nursing or any other similar field and are interested in be...

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University degree

1500 h

Online

60 ECTS (Créditos)

Titulacion

Qualification of Master of Continuing Education in Clinical Trials Monitoring and Pharmaceutical Development

Double Degree:

  • University's own Master's Degree in Continuing Education in Clinical Trial Monitoring and Pharmaceutical Development issued by the Antonio de Nebrija University with 60 ECTS credits.
  • Proper University Degree of Master of Continuing Education in Monitoring of Clinical Trials and Pharmaceutical Development, issued and endorsed by the European Institute of Business Studies.(INESEM) "Non-official education and not conducive to obtaining a degree with official status or certificate of professionalism."
  • European Institute of Business Studies

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Universidad Antonio de Nebrija

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Objectives

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Know and understand all stages of drug development.

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Manage the regulatory aspects of clinical trials.

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Obtain a broad vision of the pharmaceutical industry and its relationship with marketing and pharmacoeconomics.

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Content

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Methodology

Con nuestra metodología de aprendizaje online, el alumno comienza su andadura en INESEM Business School a través de un campus virtual diseñado exclusivamente para desarrollar el itinerario formativo con el objetivo de mejorar su perfil profesional. El alumno debe avanzar de manera autónoma a lo largo de las diferentes unidades didácticas así como realizar las actividades y autoevaluaciones correspondientes. La carga de horas de la acción formativa comprende las diferentes actividades que el alumno realiza a lo largo de su itinerario. Las horas de teleformación realizadas en el Campus Virtual se complementan con el trabajo autónomo del alumno, la comunicación con el docente, las actividades y lecturas complementarias y la labor de investigación y creación asociada a los proyectos. Para obtener la titulación el alumno debe aprobar todas la autoevaluaciones y exámenes y visualizar al menos el 100% de los contenidos de la plataforma. El Proyecto Fin de Máster se realiza tras finalizar el contenido teórico-práctico en el Campus. Para aprobarlo es necesaria una nota mínima de 5. Por último, es necesario notificar la finalización del Máster desde la plataforma para comenzar la expedición del título.

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What does it prepare you for?

With this Master in Clinical Trial Monitoring and Pharmaceutical Development you will get the necessary tools to follow up and monitor clinical trials. It prepares you to work in Contract Research Organizations (CROs), pharmaceutical industry research groups, hospitals and biomedical foundations. Develop yourself as a professional in the pharmaceutical industry and contribute to the scientific advances of the future.

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Who is it aimed at?

This Master in Clinical Trial Monitoring and Pharmaceutical Development is aimed at those who have a university degree in health sciences, either pharmacy, medicine, chemistry, biology, nursing or any other similar field and are interested in being part of drug development, being part of the research in the clinical phases of the study of drugs.

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Career opportunities

This Master in Clinical Trial Monitoring and Pharmaceutical Development trains students to enter the field of clinical trials in different profiles, either as Clinical Trial Monitor (CRA), Clinical Trial Coordinator (SC), Clinical Trial Assistant (CTA), Medical Advisor (MA) and other similar positions in the pharmaceutical industry.

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