Master in ricerca clinica - i livello
1st level vocational master
A.Y. 2023/2024
Study area
Medicine and Healthcare
Master Coordinator
Clinical research brings about a need for specialised staff, therefore requiring the creation of new professions.
The vocational master programme in Clinical Research is geared towards physicians, biologists, biotechnologists, pharmacists, nurses, physical therapists and computer scientists who are interested in receiving specialised training, to become qualified professionals at different levels and take on the many roles needed in the framework of clinical research studies. The goal of the programme is to provide theoretical and practical tools to enable students to define the rationale of a clinical study, choose the most suitable methodology, plan a research protocol, follow and coordinate the different stages of a clinical study, and properly interpret and disseminate its results.
By the end of the programme, students should be able to: formulate research questions/hypotheses properly; choose and design a suitable study to investigate such hypothesis and answer such questions; plan, coordinate and supervise the various stages of epidemiological studies and clinical trials. Moreover, they will learn how to apply clinical and epidemiological methodologies in different settings and thoroughly collect data for statistical analyses. Lastly, they will be able to critically assess results and properly communicate them to the scientific community.
The vocational master programme in Clinical Research is geared towards physicians, biologists, biotechnologists, pharmacists, nurses, physical therapists and computer scientists who are interested in receiving specialised training, to become qualified professionals at different levels and take on the many roles needed in the framework of clinical research studies. The goal of the programme is to provide theoretical and practical tools to enable students to define the rationale of a clinical study, choose the most suitable methodology, plan a research protocol, follow and coordinate the different stages of a clinical study, and properly interpret and disseminate its results.
By the end of the programme, students should be able to: formulate research questions/hypotheses properly; choose and design a suitable study to investigate such hypothesis and answer such questions; plan, coordinate and supervise the various stages of epidemiological studies and clinical trials. Moreover, they will learn how to apply clinical and epidemiological methodologies in different settings and thoroughly collect data for statistical analyses. Lastly, they will be able to critically assess results and properly communicate them to the scientific community.
To be eligible for the programme, candidates must hold a Bachelor's degree in one of the following classes pursuant to Ministerial Decree 270/2004: L-2 Biotechnologies; L-13 Biology; L-31 Computer science; L-32 Environmental sciences; L-41 Statistics; LM-13 Pharmacy and Industrial Pharmacy; LM-41 Medicine; L/SNT1 Nursing and midwifery (only the Bachelor's degree in Nursing is accepted); L/SNT2 Health professions for rehabilitation (only the Bachelor's degree in Physiotherapy is accepted); L/SNT3 Health professions for technical assistance (only the Bachelor's degrees in Cardiocirculatory and Cardiovascular Perfusion techniques, Biomedical Laboratory techniques and Imaging and Radiotherapy techniques are accepted).
The programme is designed for anyone wishing to update their expertise to be able to plan, design, coordinate and supervise non-profit and sponsored clinical studies at public or private healthcare facilities, or within the medical departments of pharma and biotech companies.
Career prospects are diverse and include working in companies or research groups involved in the design, coordination and monitoring of clinical studies, as well as in the analysis and dissemination of research results.
Career prospects are diverse and include working in companies or research groups involved in the design, coordination and monitoring of clinical studies, as well as in the analysis and dissemination of research results.
Department of Pathophysiology and Transplantation, 9 Pace Rd., Milan (IT) 20122
- Department of Pathophysiology and Transplantation.
via Pace n. 9 - 20122 Milano
[email protected]
+390255033447 - fax 0254125100
Courses list
Open sessions
| Courses or activities | Professor(s) | ECTS | Total hours | Language |
|---|---|---|---|---|
| Compulsory | ||||
| Clinical Research Methodology | 9 | 90 | Italian | |
| Clinical Trial of Medical Devices and Applicable Rules | 1 | 10 | Italian | |
| Gene Therapy: Safety, Rules Established By the Italian Medicines Agency (AIFA) | 1 | 10 | Italian | |
| Legislation and Bioethics | 3 | 30 | Italian | |
| Other Aspects of Clinical Research | 2 | 20 | Italian | |
| Pharmacogenetics and Pharmacogenomics | 1 | 10 | Italian | |
| Planning and Organising a Clinical Trial | 4 | 40 | Italian | |
| Practical Exercises in Department's Laboratories | 14 | 240 | Italian | |
| Safety Profile Assessment of Drugs Used in Clinical Trials and Methods of Pharmacovigilance | 2 | 20 | Italian | |
| Statistics Applied to Clinical Research | 2 | 20 | Italian | |
| Therapeutic Equivalence Studies | 1 | 10 | Italian | |
Enrolment
Places available: 18
Call for applications
Please refer to the call for admission test dates and contents, and how to register.
Application for admission: from 07/07/2023 to 09/10/2023
Application for matriculation: from 24/10/2023 to 31/10/2023
Attachments and documents
Please note
Deadline for call: 9 october 2023