MEDICAL AND HEALTH

INTERUNIVERSITARIO - MTEA - Medicina dei trapianti ed epatologia avanzata


luogo-corsoMonza - Padova
livello-corsoMaster 2 Level
lingua-corsoItalian
durata-corso12 months
presenza-corsoblended
APPLICATION DEADLINE
26 Sep 2025
PLACES AVAILABLE
20

DURATION

From
Nov
11
2025
To
Oct
31
2026

€ 4.000

What skills do you gain?

Elementi di terapia immunosoppressiva
Tecnica chirurgica dei trapianti d'organo
Indicazioni e controindicazioni
Gestione della lista d'attesa
Aspetti intensivi e radiologia interventistica
Le complicanze che seguono il trapianto
La recidiva di malattia e il ritrapianto
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Professional opportunities

immagine sbocco

Corso Executive in Child Safeguarding Policy

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. 

Autore: admin
ECONOMIC, STATISTICS AND LAW

Data Management for Clinical Research


luogo-corsoMilano
livello-corsoMaster 1 Level
lingua-corsoItalian
durata-corso12 months
presenza-corsoblended
APPLICATION DEADLINE
10 Oct 2025
PLACES AVAILABLE
30

DURATION

From
Nov
14
2025
To
Nov
13
2026

€ 3.500

What skills do you gain?

Clinical research methodology
Informatic tools for clinical research
Operational aspects in clinical research
Data management nella ricerca clinica
Data science for clinical research
Data science per la ricerca clinica
Integrative activities
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Data Management for Clinical Research

Who is it aimed at ?

neolaureati
RECENT GRADUATES
Bachelor’s and Master’s degree graduates from all disciplines.
professionisti
PROFESSIONALS
in the field of clinical research

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.

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Professional opportunities

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Clinical Research Coordinator (CRC)

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.

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Clinical Research Associate (CRA) o Monitor

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.

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Clinical Data Manager (CDM)

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.

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Clinical Trial Assistant (CTA) e Start Up Specialist

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.

immagine-docenteBARBARA BALCONI

Il Ruolo e le Funzioni del Tutor nella Scuola


luogo-corsoMilano
livello-corsoTraining Course
lingua-corsoItalian
durata-corso7 months
presenza-corsoIn presence
APPLICATION DEADLINE
17 Oct 2025
PLACES AVAILABLE
30

DURATION

From
Nov
27
2025
To
Jun
30
2026

€ 350

immagine-docenteFRANCESCA GRANUCCI

The power of advanced multiplexed imaging


luogo-corsoMilan
livello-corsoExecutive Course
lingua-corsoEnglish
durata-corso44 hours
presenza-corsoIn presence
APPLICATION DEADLINE
19 Jun 2025
PLACES AVAILABLE
16
APPLICATION CLOSED

DURATION

From
Jun
30
2025
To
Jul
04
2025

€ 500

immagine-docenteTIZIANA VETTOR

La professione dell'Agente Sportivo. Corso per l'Esame di Agente Sportivo (CEAS)


luogo-corsoOnline
livello-corsoExecutive Course
lingua-corsoItalian
durata-corso80 hours
presenza-corsoe-learning
APPLICATION DEADLINE
03 Nov 2025
PLACES AVAILABLE
35

DURATION

From
Nov
14
2025
To
Jan
31
2026

€ 800

immagine-docenteANTONIO PRUNAS

ECM P11 Introduzione alla psicoterapia affermativa per persone LGBTQIA+


luogo-corsoMilano
livello-corsoECM Course
lingua-corsoItalian
durata-corso16 hours
presenza-corsoblended
APPLICATION DEADLINE
09 Jun 2025
PLACES AVAILABLE
200
APPLICATION CLOSED

DURATION

From
Jul
04
2025
To
Jul
05
2025

€ 200 con ECM

€ 150 senza ECM
immagine-docentePROF. ANTONIO PRUNAS

ECM P10 La persona trans e gender-diverse in consultazione


luogo-corsoMilano
livello-corsoECM Course
lingua-corsoItalian
durata-corso48 hours
presenza-corsoblended
APPLICATION DEADLINE
30 Aug 2025
PLACES AVAILABLE
200
APPLICATION CLOSED

DURATION

From
Sep
26
2025
To
Nov
22
2025

€ 400 con ECM

€ 300 senza ECM
immagine-docenteELISABETTA BIFFI

Strategies and practices of advocacy and children’s participation: the profile of the Child Safeguarding Officer


luogo-corsoMilano
livello-corsoExecutive Course
lingua-corsoItalian
durata-corso40 hours
presenza-corsoe-learning
APPLICATION DEADLINE
22 Sep 2025
PLACES AVAILABLE
25

DURATION

From
Oct
03
2025
To
Nov
08
2025

€ 400

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Galileo Festival

The Galileo Festival Academy returns this year, offering a unique opportunity for university students to participate in the Galileo Festival of Science and Innovation, scheduled in Padua from May 9 to 11, 2025.

Selected students will take part in company visits and festival events, engaging with entrepreneurs, researchers, and industry experts.

How to Apply, Available options:

Option 1: Company visits + Galileo Festival (May 8-11)

Option 2: Galileo Festival only (May 9-11)

The first application deadline is February 23, 2025.

Autore: admin