Master in Permanent Training in Management and Monitoring of Clinical Trials

1. Training and specialization

The development of new drugs and therapies is a very important activity that offers the possibility of generating new treatments for patients and promoting medical-scientific progress.

The necessary investment in research and development that this entails within the pharmaceutical, biologics and medical device industries, together with the increasing emergence of new biotech companies, has helped create new career opportunities in the healthcare world.

Increasing regulatory demands, technological and scientific advances, as well as new treatment modalities in an increasingly competitive environment, have accelerated the demand for professionals trained and specialized in clinical trials.

The Master in Clinical Trial Management and Monitoring has been created in response to this growing need in the health research environment, both in the pharmaceutical industry and in Clinical Research Organizations (CRO), biotechnology and medical device companies, research, foundations and hospitals, which participate in the development of these new drugs and therapies.

2. Program developed with Experior

Program developed with Experior, one of the leading national companies in the clinical trials market based in Valencia, and which has more than five years' experience coordinating the scientific and internship part of postgraduate degrees in this area.

3. Eminently practical approach

The main objective of the master's degree is for students to begin their professional career immediately and safely after completing the degree. This is achieved thanks to its eminently practical approach, with a six-month internship module in companies and institutions of recognized prestige in the sector.

4. Specialized knowledge and skills

Of a multidisciplinary nature, necessary to understand, supervise and manage clinical trials. Provide the knowledge and skills that allow an effective response to the continuous changes in clinical trials in a context of transformation subject to the results of the latest research carried out and to local, national and international legislation.

Students will develop the knowledge and skills that will allow them to effectively start their professional development within the field of clinical research.

Motivate students to apply the knowledge and skills acquired to influence the development of new activities within clinical research.

Provide the ability to critically evaluate clinical trial processes, taking into account ethical aspects, in the current legislative and health environment.

5. Collaborators from different disciplines

The Master has a faculty of collaborators from different disciplines who combine the language of daily practice with the academic rigor of the University. The diverse origin of the teaching staff ensures both a public and private approach, with which the student is provided with a much broader vision of the current and future reality of the topics covered in the program and their application in day-to-day reality.