Clinical Assistant Online Course: Master in Clinical Trial Assistant + University Degree (5 ECTS credits)

In a scenario where clinical trials are vital for medical advances, the role of the Trial Assistant clinical becomes a cornerstone of this process. Our Master in Clinical Trial Assistant offers comprehensive training, covering from health administration to the implementation of quality systems in laboratories. Through a agenda that encompasses the management of health documentation and clinical trials, together with laboratory biosafety, the program prepares professionals to face the current challenges of the sector. This course, arranged entirely online, is designed to strengthen key skills that the industry demands, such as meticulousness in document management and the ability to operate under regulations such as ISO 17025. Although continuous training does not directly enable to work, this course enriches the student's profile, expanding their theoretical understanding, which is crucial for effective professional development. Thus, this master is a preferential option for its news and applicability in the field of medicine and research.

- Dominate sanitary administrative management. - Manage clinical documentation effectively. - Apply regulations in clinical trials. - Implement ISO 17025 quality in LAB. - Manage biosecurity and occupational hazards. - Understand accreditation in laboratories. - Organize waste in clinical environment.

The Master in Clinical Trial Assistant opens doors to professionals in the health and research sector. Graduates may manage clinical documentation and articulate quality systems according to ISO 17025 in laboratories. They will specialize in biosafety and risk prevention, enhancing their profile in laboratory accreditation, clinical trials and health administration, marking a trajectory in the avant -garde of medical research and the improvement of procedures in health environments.

The Master in Clinical Trial Assistant expands your skills in the field of clinical trials and their administration. It enables you to solve with solvency the documentation and health management, as well as the specificities of the clinical trials. It covers from the implementation of quality systems according to ISO 17025, to laboratory biosafety strategies and occupational risk prevention. This knowledge positions you to be a valuable collaborator in research and development teams, although regulated training is essential to exercise.

This Master in Clinical Trial Assistant is designed for health personnel, researchers and laboratory technicians interested in deepening the management of clinical trials and quality in laboratories with ISO 17025. Ideal for those who seek to complement their training in biosafety, health and administrative documentation, and prevention of occupational hazards, without this implying training to exercise without regulated degree.

This training is not included in the scope of official regulated training (Infant Education, Primary Education, Secondary Education, Official Professional Training FP, Baccalaureate, University Degree, Official University Master and PhD). It is therefore a complementary and/or specialization training, aimed at acquiring certain skills, skills or aptitudes of a professional nature, being able to be barely as merit in workbags and/or opposition competitions, always within the complementary training section and/or continuous training being always essential to review the specific requirements of the public labor stock of the public labor stock market.