
This Master 2 program focuses on clinical research, offering a curriculum designed to train high-level professionals for roles in clinical studies. It combines academic learning with practical experience through an apprenticeship model. The program emphasizes the skills needed for designing and managing clinical trials, adhering to regulatory standards and data security. The course is taught by a faculty composed of researchers and industry professionals from the pharmaceutical, medical device, and contract research organization sectors. The learning approach is innovative and tailored to the demands of alternating study and work. Students receive close supervision from both academic staff and their company mentors. This Master's degree is particularly relevant for those seeking careers in clinical trial management, data analysis, and regulatory affairs within the healthcare industry. It integrates knowledge from related fields like toxicology, machine learning, and cybersecurity to provide a comprehensive understanding of modern clinical research.
The Master 2 program includes 508 hours of theoretical training divided into 10 teaching units, covering a wide range of essential topics in clinical development and research.
Graduates of this program are prepared for a variety of key roles in the clinical research sector, contributing to the development and management of clinical trials.
Applicants must be under 30 years old to be eligible for an apprenticeship contract.
As this is an apprenticeship program ('Formation en Apprentissage'), tuition fees are typically covered by the employer through the apprenticeship contract. Specific details would be clarified during the application process.
This program is part of the offerings from Paris Cité University.
To be eligible, applicants must be under 30 years old and have completed a Master 1 in relevant fields like Toxicology, Data Science, Cybersecurity, or Biomedical Sciences. Equivalently, completion of the 5th year of Pharmacy or 4th year of Medical studies is also accepted.
This is an apprenticeship program, so tuition fees are typically covered by the employer through an apprenticeship contract. Specific details regarding financial arrangements will be clarified during the application process.
The program involves 508 hours of theoretical training spread across 10 teaching units. It is structured as an apprenticeship, combining academic learning with practical experience.
Graduates are prepared for roles such as Clinical Research Associate (ARC), ARC Manager, Clinical Study Coordinator, and Clinical Study Operations Manager/Clinical Project Manager in the clinical research sector.
Applications are submitted through the CFA Leem website. The selection process includes reviewing your application dossier and attending a selection interview.