You want to become CRA and you wonder what training to follow to achieve it? You are a little lost in the different ways to get this profession? It is to be noticed that many different types of training exist to become CRA: private, intensive or not, public training, learning, and internship … To help you, you will find a list of different trainings that exist and their characteristics.
To become a CRA you must preferably get scientific basis: most of CRAs possess a medical or biology training. However, it is possible to do this profession with another initial training. From high school degree +3 to +8, the CRAs generally have a high school degree +5. Namely: your experience will be more considered than your training.
If you are currently working in the pharmaceutical industry, you also have the opportunity to perform the CRA after a CRA training. You have several options: continuing training, if you want to achieve a high school degree +5 level for example or a CRA degree.
If you have an extensive experience in the field of health (as a lab technician, nurse, health visitor…) you can reorient yourself by getting a CRA degree.
Masters are rather for university training people (orientation at the end of the bachelor degree or M1 for example). If your pharmaceutical company agrees, masters are also available in continuing training, but be careful as places are often limited.
There are several specialized professional masters in clinical research, we have decided to present three of them.
- Professional and Research Master, health sciences biology of drug, specialty: clinical trials and drug development – University of Poitiers
To access the Master 1, you must have validated a general license in line with the theme of the master, that is to say, physiology, pharmacology, biology…
To access to Master 2, you must have validated the M1 above or exceptionally another M1 whose content is adapted to the continuation in M2, or the 5th year of Pharmacy or medicine study.
Internships / learning:
- 1st internship planned in semester 2 of M1: 8 to 12 weeks
- 2nd internship planned in Semester 2 M2 18 to 24 weeks
In the program:
In M1: Genomics and Bioinformatics Tools, interpretation tools of biological images, Epidemiology, Regulatory Environment and Development of Medicine, Pharmacology and Toxicology, quality study and healthcare industries, English, Biostatistics,
SAS Programming, Experimental Cell Physiopathology of Major Functions, Introduction to Data Management, Advanced Databases and Applications, Clinical Physiopathology, from laboratory to patient’s bed and vice versa.
M2: Clinical Trials Methodology, Implementation, Management and Regulation of Clinical Trials, Clinical Trials Environment, Clinical Epidemiology, Outcomes and Pharmacology and economics, Corporate Culture and Communication, English (TOEIC on request), clinical project management.
The subjects are varied and related to different fields: methodology, statistical … This Master will enable you to work as CRA, but also other works. The master offers you the possibility to perform different types of professions in the research field and health economics. It is up to you to choose your internships in order to aquire relevant experience for the profession you want to perform later.
For more information on this master click in the Université de Poitiers.
Master 1 Biology Specialty Health “Health Professions associated with clinical research” and Master 2 professional Clinical Evaluation of Therapeutic Trials – University of Montpellier
To access to Master 1, you must have a validated L3 of Science or Health Engineering, be clinical psychologist or have validated Pharmacy or Medicine studies.
To access to Master 2, you must have validated the Master 1 “Health Professionals applied to clinical research” at the University of Montpellier or Master 1 of Biology, be a health professional, physician, pharmacist or scientist. This training is also available through continuing training. In this case, you must be an employee of a pharmaceutical company.
Internships / learning:
This master is interspersed with several courses:
- 1 internship planned in Semester 2 of M1.
- 2 hospital internships for 3 months in M2: presence in internship in the morning and during the afternoon.
Students should choose this internship depending on the specialty in which they would like to move. The internships take place at the Montpellier CHU (University Hospital Center).
- In the second part of the year in M2: an industrial internship of 6 months. The University has partnerships with laboratories, CROs and associations.
This organization will allow you to discover different ways of working in clinical research: in hospital or in CRO / laboratory.
In the program:
M1: technical and regulatory and financial aspects – environmental health, English,Laws in Environmental Health Basics, Toxicology Investigation, parametric and non-parametric statistics, information and database systems, and statistics applied to biology, entrepreneurial initiative, and Intellectual Property.
M2: Project Management, Operational Planning, Financial Analysis, Health Economics, Specials clinical trials in each medical specialty, methodology and biostatistics, design of new therapies and clinical evaluation of biotherapies, …
This master trains to the professions such as CRA Coordinator, CRA manager, Quality Manager, Regulatory Affairs Manager … The Master seems more oriented to allow you to access the project manager profession. You can consider this master to move quickly to project management positions.
For more information on the master:
– Master 2 Professional Coordinator of studies in the field of health – University of Versailles – Saint-Quentin-en-Yvelines
To access to this master, you must have validated a Master 1 of Biology or equivalent. Admission is done by application followed by an interview.
Internships / learning:
This master is completed in learning if you are under 26 years old (age limitation for an apprenticeship) or for some students as part of continuous training. The university has partnerships with private companies: laboratories or CRO and associative hospitals or Public Hospitals of Paris in Ile de France and elsewhere in France (Amiens, Dijon, Lille, Lyon, and Montpellier).
The alternation will take place as follows: 8 periods of two weeks at university, spaced of 4 to 5 weeks in a company.
In the program:
Medicine and Clinical Research: Pathology, clinical trials methodology, statistics and databases, epidemiology and public health, GCPs and accreditation, galenic forms, risk management plan.
Law and Ethics: French and EU in the field of health and biomedical research, Law of intellectual property and patents, law, ethics and legal procedures: Ethics Committee, CNIL, CCTIRS “Medical ethics and experimentation on humans.
Management and Project Management, Health Economics and Research, English (TOEIC on request), Knowledge of the hospital, relevant search data in medical records.
This Master will enable you to become CRA and CRA coordinator but also to engage in other professions of clinical research, economic evaluation or quality control, communication in the field of clinical research or paramedical and health Public.
For more information on the master: http://www.etu.uvsq.fr/master-2-professionnel-coordinateur-d-etudes-dans-le-domaine-de-lasante-60332.kjsp
The masters offer you a bachelor degree +5 level that will have an impact on your wages (especially in hospitals). They also allow you to evolve as CRA Coordinator, Project Manager, Head of Regulatory Affairs, etc. However, it is often necessary and advisable to start as CRA to gain field experience.
III. Other courses
Other courses are faster than Masters (from weeks to 1 year). However, you are more independent than you are in the context of a master.
The CRAT IUD: “Clinical Research Associate and Clinical Study Technicians Training” Inter-University Diploma.
Prerequisites: requirements vary depending on the university in which you will register. You should preferably have professional experience in the field of pharmacy and health: nurses, laboratory technicians … but some courses are also open from the bachelor degree +2 level.
Training is also available to those in continuing training.
Internships / learning: the internship is not mandatory but on request. It is even strongly recommended! It alone will allow you to gain initial experience in this field if you do not have.
On the program: 15 to 20 days during 1 year (1 day / week, as 5-day sessions)
Methodological basis of clinical trials, logistics and follow-up of trials, Structure and Organization of Public and Private Biomedical Research, General Basis of oral and written communication in the trials, pharmacovigilance, risk management and vigilance in the trials, management of resource biological centers …
The program also depends on the university. However, the basics of the program remain much the same.
Registration fees: fees vary between € 450 and € 700 for initial training according to the chosen university.
The universities offering this degree are: Paris VI, Paris VII, Continue training Mixed Unit in Health Aix-Marseille University, Bordeaux II, Lyon I, Nantes, Strasbourg (courses in Strasbourg and Nancy)
Sup Santé: https://www.supsante.com/formation-continue/attache-recherche-clinique.cfm
Prerequisites: from a scientific Bachelor degree +4, medical Visitors with 3 years of professional experience, people in continuous training.
English knowledge and license B.
Training / Learning: obligatory practice internship of 4 to 6 months.
In the program: on 3 months.
Science Education (Cardiology, Urology, Nephrology, Gastroenterology, Hepatology, Pneumology, Oncology, Pharmacology, Infectious Diseases, Endocrinology, Psychiatry) Professional education: Terminology, Clinical research and development studies, GCPs, The Clinical Research Associate, Visits, Regulatory, Quality Assurance.
Some courses are in English.
Registration fee: € 4000
For more information on this, click in sup santé
Prerequisites: Bachelor degree +3 in science, initial health training or significant experience.
Internship / Learning: No compulsory internship but possibility to do an internship at the end of training.
In the program: on 1 month
Clinical Research: French and international regulations, The CRA profession, the Project Management and Methodology, Clinical monitoring on-site and remotely, e-Learning Tools: eCRF, eCRF Generator, CTMS, pharmacovigilance and materiovigilance, clinical research impact in the drug and medical device addressing current therapeutic issues, Establishment of a clinical trial, cross-management of a clinical trial.
Training Cost: € 2,730
These trainings are quick and complete for the CRA profession. In addition, they offer internships that will allow you to gain your first experience as CRA.
For more information, click on the Clinact link
The choice of your training to become CRA will therefore shift according to your initial training, your time, and your budget. Do not hesitate to talk with the training managers to make your choice knowingly. Favor trainings with which you will have the opportunity to do an internship or better apprenticeships. However, in case of dual training, pay attention to the rhythm of alternation. Indeed, the rythm can sometimes be restrictive and prevents you from keeping track of a single project. In this case, you will work on projects to the needs of your employer.
Recruiters will pay attention to your practical experience rather than your initial training (if practical experience exist). You have all the keys in hand to choose your training and become CRA, now for you to start!
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