Milan
Master 1 Level
Italian
12 months
blended
The Master’s program aims to train professionals capable of independently managing all aspects related to social responsibility and sustainability within companies, public administration, and the non-profit sector.
Thanks to a strongly multidisciplinary approach, participants will develop the ability to navigate various social responsibility management strategies and to independently implement the legal, administrative, and accounting procedures currently required by law or made indispensable by ethical considerations and the expectations of consumers and stakeholders, particularly in internationalization processes.
The training need in this subject stems from the requirement for companies and organizations to develop the capacity to manage a variety of procedures recently introduced at the global, European Union, and national levels, which are currently not covered by traditional university curricula.
The very nature of these procedures (due diligence plans; environmental and social impact assessments; supply chain control systems; preparation of accounting documents containing non-financial information, etc.) necessitates a teaching approach strongly characterized by the collaboration of academic faculty with high-level experts and professionals from regulatory bodies and businesses.
This course has adopted this approach and further enriches the learning path by offering seminars aimed at developing so-called soft skills; support for project work activities; and participation in company internships.
Upon completion of the Master’s program, participants—being experts in sustainability and social responsibility topics—will be qualified to manage these issues within professional and consulting firms, in various organizational departments of private companies and public entities, or to independently formulate the CSR policy of an organization, or even to establish and lead an autonomous department dedicated to managing related matters.
The Master's program aims to train professionals capable of independently managing all aspects related to social responsibility and sustainability within companies, public administration, and the non-profit sector.
Thanks to a strongly multidisciplinary approach, participants will develop the ability to navigate various social responsibility management strategies and to independently implement the legal, administrative, and accounting procedures currently required by law, aimed at achieving sustainable management of resources and economic and administrative activities.
320 hours of lessons
375 hours of Stage/Project Work
The decision to target the Master’s program to a wide range of participants is driven by the fact that the skills offered have become essential in every professional field.
The Master’s program organizes interviews with partner companies to facilitate job placement. The broad application of the skills taught and the high demand for experts in the field have enabled participants from previous editions to secure prominent positions in corporate management across various roles.
Various roles related to sustainability and social responsibility, which are experiencing significant growth across all sectors.
Clicca qui per la testimonianza
Clicca qui per la testimonianza
Clicca qui per la testimonianza
Fabio Prete, funzionario della Camera di Commercio di Milano – Albo Nazionale Gestori Ambientali, racconta qui la sua esperienza come ex allievo del Master di I livello “La professione per la Sostenibilità: Aspetti Legali, di Finanza e Management – SiLFiM” di Bicocca Academy
Milano
Professional training
Italian
8 months
blended
Corso Interuniversitario con Universidad de Buenos Aires.
Il corso intende fornire un'ampia rassegna della strumentazione critica offerta dalle scienze umane contemporanee, dall'antropologia alla sociologia, dalla teoria della storia all'economia politica, dalla psiconalisi alla filosofia, dai gender studies ai postcolonial studies. L'obiettivo fondamentale è quello di formare uno sguardo capace di cogliere i nessi profondi della crisi contemporanea attraverso un'apertura ad un sapere interdisciplinare ed ad un'attitudine che sappia valorizzare la grande tradizione della critica della società.
Le competenze fornite nel corso possono risultare fondamentali come formazione e completamento per l'attività in ruoli politici e sindacali di vario livello, nelle realtà associazionali e nel settore no‐profit, nonché come integrazione della preparazione all'attività giornalistica nelle specializzazioni più legate all'analisi politico‐sociale. Il corso costituisce anche un valido aggiornamento per l'attività di insegnamento nelle scuole superiori e più in generale per tutte le professioni pedagogiche.
The lessons will be available both in-person and remotely, in asynchronous mode.
Students wishing to also obtain the degree from the equivalent course held at the University of Buenos Aires (UBA) must replace 9 ECTS credits from our course with an equal number of courses from the UBA program. UBA lessons can be accessed via e-learning (live or asynchronous) on our platform or attended in person at UBA. Travel, food, and accommodation expenses are the responsibility of the student. A prerequisite is knowledge of the Spanish language.
232 hours of Lessons
Attempts to reinterpret Western aesthetic philosophy through critical categories from postcolonial theory and Black studies (Lloyd, Black).
Monza - Padova
Master 2 Level
Italian
12 months
blended
La Medicina dei trapianti d’organo rappresenta una delle principali conquiste della medicina moderna e risulta essere l’unico approccio curativo per un numero crescente di condizioni cliniche che portano alla insufficienza acuta o cronica d'organo. Il successo di questa terapia ha portato ad un costante incremento del numero di trapianti effettuati, ma anche al concomitante incremento delle lista d’attesa, stimolando la ricerca di innovazioni biologiche e chirurgiche atte ad aumentare la disponibilità di organi ed ottimizzare i risultati.
La Medicina del trapianto richiede conoscenze altamente specifiche, venendosi sempre di più a configurare come una branca a sé. Infatti i medici coinvolti nei Centri Trapianto devono:
l grande successo dei trapianti d’organo come terapia delle insufficienze d’organo terminali ha causato il continuo aumento del numero dipazienti che hanno subito un trapianto e pertanto della domanda sanitaria.
Il master si propone di:
460 hours of Didattica Frontale
1040 hours of studio individuale + stage
Registration is now open for the Bicocca Academy Executive Course "Strategies and practices of advocacy and participation of minors: the role of the Child Safeguarding Officer", directed by Prof. Elisabetta Biffi, a high-level training course dedicated to the protection and promotion of children's rights in public and private organizational contexts.
Milano
Master 1 Level
Italian
12 months
blended
Since the scientific validity of a clinical study depends on the methodological rigor of the protocol, compliance with the procedures it describes, and the quality of the data on which the analysis of results is based, the role of the Data Manager has become increasingly essential across public and private organizations engaged in planning, conducting, and evaluating clinical research. This professional figure is indispensable for carrying out all activities related to the management of clinical data and documents that, throughout a clinical study, must be prepared by investigators, ethics committees, sponsoring companies, CROs, and data processing centers.
Participation in the Master’s program allows students to obtain the Good Clinical Practice ICH-GCP E6 certification.
The overall educational goal of this Master’s program is to provide highly qualified training for the following functions:
The Master’s program is designed to ensure that students acquire:
The 304 hours of lessons planned in the curriculum are delivered as follows:
The majority of lessons are provided remotely in a blended format, either synchronously (via the Webex platform) or asynchronously (through video lectures and exercises made available to students on the Master’s e-learning portal);
Approximately 30% of the lesson and exercise hours—including 28 hours dedicated to REDCap software training and 28 hours to SAS training—are delivered in person in computer-equipped classrooms at the University.
All synchronous remote lessons are recorded and made available to students through the Master’s e-learning portal. Webex streaming recordings are considered supplementary teaching materials and do not replace participation in live synchronous lessons.
304 hours of Lezione
500 hours of Stage/Project Work
The final exam consists of an oral discussion of the internship/project work.
Drug development phases
Types of clinical studies
Experimental designs, observational designs, adaptive designs
Uncertainty in the diagnostic process
Frequency of clinical events
Random and systematic errors in diagnostic measurements
Bias control
Systematic reviews and meta-analyses
Introduction to relational databases
Conceptual design
Logical design
SQL language
Good Clinical Practice (ICH-GCP R3)
Regulatory framework (observational studies and interventional studies with drugs and medical devices)
Ethical and regulatory evaluation and authorization process of a clinical trial
Clinical trial monitoring
Data governance
Quality requirements in clinical trials
Principles of Computer System Validation (CSV) in the GCP context
Elements of project management and performance indicators
Tools for data collection (CRFs/eCRFs, study database, and other important data)
Cleaning of efficacy and tolerability data
Processes for coding drugs and medical terms
Reconciliation of the study database with the pharmacovigilance database (serious adverse events)
Interaction with the study team for study progress control and data quality monitoring
Importance of clinical data management systems
Introduction to the REDCap system: Piping/Smart Variables/TAGs, Branching Logic, Project HOME/SETUP/Applications (tools), randomization
Introduction to SAS programming language
Procedures for data import
Creation of derived variables
Main procedures for data validation
The importance of biostatistics in clinical research
Elements of descriptive and inferential statistics
Methods for analyzing continuous, categorical, and survival outcomes
Introduction to machine learning
Building machine learning pipelines through visual interaction using the OrangeML suite
The Clinical Research Data Manager is a key figure in the planning and conduct of clinical research studies. Their expertise applies to both commercial (Profit) and non-commercial (Non-Profit) research.
This professional role is responsible for managing and coordinating clinical studies, usually at the investigative site. The CRC assists researchers and study staff in planning, organizing, and supervising activities related to clinical studies, while ensuring coordination of activities and maintaining communication with Monitors and Sponsors. Responsibilities include managing study documents, recruiting and managing participants, handling data at the clinical investigative site, communicating with various stakeholders, and monitoring study progress to ensure that all procedures are conducted in compliance with protocols and applicable regulations.
The Clinical Research Associate (CRA), also known as Monitor, is responsible for overseeing clinical studies to ensure they are conducted in compliance with protocols, Good Clinical Practice (GCP), and applicable regulations. This role includes verifying data collection, monitoring ethical and regulatory compliance, and supporting research sites participating in the study to resolve any operational issues. Typically, the CRA works on behalf of the clinical trial sponsor, whether profit or non-profit (e.g., pharmaceutical companies, CROs, non-profit organizations, etc.).
The Master’s program provides the theoretical training required by the decree of November 15, 2011 (known as the CRO decree), as well as the foundational knowledge necessary for this professional activity. However, the practical monitoring experience—mentored alongside an experienced Monitor at clinical research sites—is essential for CRA certification. This hands-on training depends on the host organization where the student undertakes their internship and is rarely guaranteed.
The Clinical Data Manager (CDM) is responsible for the collection and management of data derived from clinical studies and ensures data quality and integrity. This role involves creating and maintaining clinical databases, verifying data quality and integrity, and managing data cleaning and validation processes. The CDM works closely with other members of the research team to ensure that the collected data are accurate, complete, and suitable for statistical analysis and the presentation of research results.
The Clinical Trial Assistant (CTA) is the professional responsible for supporting the Monitor and Project Manager in managing the bureaucratic and documental aspects of a clinical study, in compliance with Good Clinical Practice (GCP), internal Standard Operating Procedures (SOPs), and current regulations.
The role of the Start-Up Specialist, on the other hand, focuses on managing regulatory and authorization processes necessary for the initiation and conduct of a clinical study.
The "Operational Aspects" module of the Master, together with seminars on the practical use of the European Medicines Agency’s (EMA) Clinical Trials Information System (CTIS) platform, enables students to acquire basic regulatory and compliance skills required for entry-level positions in this field.
BARBARA BALCONI
Milano
Training Course
Italian
7 months
In presence
FRANCESCA GRANUCCI
Milan
Executive Course
English
44 hours
In presence
TIZIANA VETTOR
Online
Executive Course
Italian
80 hours
e-learning
ANTONIO PRUNAS
Milano
ECM Course
Italian
16 hours
blended
PROF. ANTONIO PRUNAS
Milano
ECM Course
Italian
48 hours
blended
