Since 2009 we provide worldwide online clinical research certification & job placement support
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For safety reasons, face-to-face consultations are not offered in the Academy till new order (building closed for quarantine). For assistance contact us by email to email@example.com, by Skype to CRA School Montreal, or by phone:
By phone: 7/7 multilingual LIVE Support : +1 (514) 257-3003
WhatsApp Support: 7/7, till 8:00 PM EST : +1 (514) 961-9351
Skype Support: by chat, 7/7, till 11:30 PM EST at CRA School Montreal
Consultations on eligibility & CV: 7/7, book a spot here and call by Skype
Education is the best investment, and to get a diploma in the comfort of your home became the new standard of learning. Already 12+ years the CRA School offers worldwide an Accredited Clinical Research Online Certification PG program with 3 remote internships in the Academy & 7/7 LIVE SUPPORT + Placement Assistance Till Hired to help students enter this ever-growing field. 1-on-1 courses for improving oral English or French are provided by Skype on request 7/7 at additional, especially reduced fees for students. Vaccine trials created a huge demand for more staff. In the 2-nd year, most of our alumni are at $80,000/yr, and today several are at rather high-level roles. See them on LinkedIn.
* * *
You think that you know GCP? Check do you know the GCP basics?
*NB: This is not an admission test, the course is open to everybody
The Accredited Clinical Research Post-graduate Certification program CRP 3.0 covers the Canadian, US, and international GCP regulations for clinical trials conduct. It is designed to support till hired professionals in career change, newcomers and aspiring Canadian Permanent Residents, who plan to settle in British Columbia, Alberta, Saskatchewan, Manitoba, Ontario, Quebec, and the Atlantic provinces, by preparing them in advance to get a job. The 40% special fee reduction is our contribution to alleviating the pandemic burden.
The combined CRP 3.0 PG course prepares students not only for the CRA role, but also for almost all jobs in this field that don’t require a license to practice, including CRC, SSU, CTA, RA, DM, and even CPM, SSM, DSA, PHV, MSL, etc. It is internationally accredited by CPD UK and recognized by TransCelerate BioPharma USA as satisfying all the requirements for mutual recognition among clinical trials sponsors of GCP training courses.
Individual, self-paced, ONLINE program with unlimited 7/7 LIVE support, adapted to the goals of every student. Share the news with friends who consider a career change, but lack the necessary tools and support and get a $100 referral bonus if anyone, whom you informed about us, enrolls someday
If you plan moving to Canada, get ready in advance with a Canadian diploma, Canadian practical experience from the internships, a network of contacts + unlimited support till hired. Very detailed program with the objective is to be fully prepared for interviews and get a job.
* PATH to Clinical Trials Jobs for international life sciences graduates:
Clinical Trials are a great alternative for foreign-trained MDs, BDS, veterinarians, pharmacists & BSc/MSc/PhD degree holders, etc
(No need for recognized diplomas, exams, nor license to practice):
* Regulatory Affairs, Data QC/QA, Drug Safety & Pharmacovigilance Jobs
* Medical Affairs roles, high wages, fast access (4-6 months detailed self-paced training with 3 remote internships & 7/7 LIVE support till hired)
*Today, most jobs became home-based. Frequent promotions due to the chronic 30% shortage of experienced staff. See more here
*Main obstacle to getting into the industry:
The law requires regulatory training AND prior experience (at least from internships). We provide both + unlimited support till hired. No time limit to finish the program.
What is different:
To make students eligible for interviews, in parallel to the regulatory ICH GCP E6(R2) course, 3 remote internships are provided in the Academy
+ active networking support allows getting job leads about the “hidden jobs” that are never posted, but filled-in by references,
+ unlimited assistance in advance for the adaptation of the CV & interview preparation for every role (till hired).
Who is eligible:
– candidates worldwide with nursing or any university degree
– research assistants, interested to join this rewarding industry
– IMG in career change (MD, DDS, DVM, BPharm, PharmD, RN)
– clinical nurses & CRC, interested to jump ships to CRA roles
What you get:
– PG Diploma of Certified Clinical Research Professional, covering all main the roles in this industry (CRC, CTA, CDM, RA, CRA)
– Hands-on experience in Canadian/US regulatory environment from 3 remote internships, including Study Management Software
– Unlimited 7/7 support from our mentors to access the hidden jobs (NB: we are not a placement company, we just assist till hired)
Who should enroll:
IMG (RN/MD/DDS/DVM/BPharm/PharmD/MSc/PhD) and any life-sciences graduates worldwide. No study permit needed. (Note that online studies do not provide students visas). Book a free consultation:
* FREE 1-ON-1 CONSULTATIONS *
Do you want to work in clinical research in Canada or
to move to Canada? Are there jobs available? How are
they paid? Are you eligible for them? Where to start?
You probably have hundreds of questions. Say “Hi” by
Skype to our account “CRA SCHOOL MONTREAL” for
any question or a free 1-hour consultation 7 days/week
or book a free consultation here. Reserve 1 hour time.
Get answers to all your questions LIVE by our expert
Discuss in detail the amazing careers opportunities
in the rewarding and booming clinical trials industry
and what would be a suitable Action Plan for you
Nurses make great Clinical Research Coordinators (CRC) and Clinical Research Associates / Monitors (CRA)
Well-known fact: Nurses are preferred for CRC & CRA roles. They know
the rules for ethical human research, the diseases, medical terminology,
and how clinics operate.
In Regulatory Affairs (RA), no medical acts are performed, so no license
to practice in the country is required. No body fluids, no night shifts.
Contact us for details on how to kick-start your clinical research career.
Get 7/7 LIVE Support till hired into the rewarding clinical trials industry.
The Accredited Postgraduate Program CRP3.0 provides GCP certification
practical experience in the clinical trials tasks, required by law, support
in building a network of contacts with hiring managers, assistance in CV
adaptation for every role, plus unlimited interview preparation till hired
Proof of qualification required at registration. Foreign diplomas accepted.
SPECIAL DEAL for foreign nurses: CAN$950.00 / US$755.00
To enroll, email your CV to firstname.lastname@example.org to assess your eligibility, and to suggest you a suitable Action Plan.
Refer a friend and get a $100 referral bonus
With the chronic 30% shortage of experienced staff, some 80-90% of the jobs are
never posted (especially the entry level jobs), but filled-in by internal promotions
and references. Companies pay a referral bonus of $1,000 up to $2,000 if they hire
the candidate that you referred. Their employees are interested to bring your CV
to the hiring manager, but they don’t know you. Hence the need to network.
As jobs are “hidden”, candidates don’t see them and these rewarding and well-paid
Regulatory Affairs jobs in the booming clinical trials industry are widely unknown.
Don’t hesitate to share this info with friends, who may profit from this opportunity.
Inform friends & colleagues about these highly-paid careers in chronic shortage
of staff, our free monthly Career events and our PG Clinical Research Certification
Onboarding program with 3 internships and Placement Support till Hired (PATH)
and get a $100 referral bonus for everyone, who enrolls in the program someday.
To register a Referral, email us the names and emails addresses of the persons
who you informed about these careers and our unique program, combining all
the tools and support needed till getting the first job.
We register them in our database to assure not to forget to pay you. The bonus
is paid in the beginning of the next month after the candidate enrolled.
The number of referrals is not limited, do not hesitate to spread the news.
Electronic Data Capture (EDC) & Clinical Trial Management
Software (CTMS) training and internship are an integral part
of the CRP3.0 Post-Graduate program. This is a major hiring
requirement. It is capital to have such practical experience.
Vaccine trials hasten the need for new clinical sites & staff.
They need 40,000+ participants, 10 times more than drugs.
This means a lot of new staff to handle this huge workload.
There have never been that many new jobs in this field. It is
the best time to go to this rewarding & blooming industry.
The CRC, CTA, & In-house CRA roles are great entry-doors to
the clinical trials field as they don’t need much prior experience
The demand of experienced staff is always high & will only grow.
Share the information with friends, who will fit and can profit.
What is new:
Get a job, not just a diploma
1) Fast access to well-paid and in-demand careers
2) International: All clinical trial careers covered
3) Internships for hands-on Canadian experience
Job-specific preparation for interviews
1) Job description analysis + CV adaptation for every job
2) Preparation for every interview until hire
3) Training in advance for topics not yet covered
Coaching & support on Professional positioning
1) Professional branding coaching & mentoring
2) Reference letters, job alerts & job assistance
3) Networking meetings & weekly consultations
Accessible when you need it
1) Online training to advance at your own speed
2) 7/7 LIVE Support by Skype till late evening
3) Flexible payment options adapted to your needs (2, 3 or 6 installments)
Job insertion support
Active Job Placement Assistance
1) Instructions on pre-selection questionnaires
2) Coaching on typical interview questions & traps
3) Introduction to industry slang & terminology
International program for all needs
1) US, Canada, EU, ICH GCP & QC regulations
2) Options for GCP professionals, MD, MSc/PhD
3) Referral Program with unlimited bonuses
The International Clinical Research Academy (the CRA School) is the only provider of international clinical research training with internships and job-placement support (Placement Assistance Til Hired; PATH program).
Our program is suitable for candidates with life science background including RN, BSc, MSc, PhD, MD, PharmD, GCP professionals, corporate staff, IRB/REB members.
Our training is universally-applicable and provides students with a solid theoretical and practical base to work in any country.
Our objective is to provide the knowledge and necessary tools that will facilitate access to rewarding careers in clinical research, including Clinical Research Associate (CRA), Clinical Research Coordinator (CRC), Clinical Trial Assistant (CTA), Study Start-Up Assistant (SSU) or Regulatory Affairs (RA).
Our courses provide the building blocks that lead to other fields including Data Management (DM), Clinical Project Management (CPM), Drug Safety Associates (DSA), Pharmacovigilance (PV), Medical-Science Liaison (MSL), etc.
Roles in clinical trials
Regulatory agencies (FDA, Health Canada or other) inspect only a small part of all studies (around 2%). The Sponsor company or individual investigator who initiates a study are obliged by law to periodically monitor the quality of the generated data and ensure that the rights and safety of the study participants are protected. The physicians (PI or sub-investigators) are responsible for the evaluation of their patients and the quality of the data
Data management, quality control & statistical treatment of study data are done by sponsor’s staff, Clinical Research Associates (CRA), in-house Monitors, Data Managers (DM), Drug Safety Associates, Medical Advisers, Biostatisticians, Project Managers and other staff trained on the study protocol, clinical trial regulations and Sponsor’s SOPs.
What is a CRA/CRC?
The Clinical Research Associate (CRA) is a monitor (inspector) who periodically visits the study sites to supervise and inspect the work of the clinical investigators and their coordinators. The CRA verifies their compliance to the protocol and the regulations, makes sure that all regulatory requirements are met and the quality of the data is acceptable. The in-house CRA or the Clinical Trial Assistant (CTA) organize all study-related activities.
The Clinical Research Coordinators (CRC) or the Clinical Research Assistants work in the medical clinics (called sites) where the studies take place. They organize all interactions with the study participants and all the study-related activities at the site. The Principal Investigator (PI) is responsible for the patients’ care, evaluations, and the conformity of all the study conduct with the law and clinical trial regulations in force.
Companies look for good communication skills in English and university diploma, which guarantees that the candidate will be able to understand a research protocol when trained. Life sciences, health care, nursing, biology, biochemistry, biomedical engineering or allied health field are preferred.
For some high-level jobs, an advanced scientific degree is required. Prior experience is always the 1st hiring criterion. The best hiring chances have professionals with some prior practical experience in clinical research activities in N.American regulatry environment.
Health professionals trained abroad often have difficulties when they move to another country. Foreign diplomas may not be recognized and the required local practical experience is missing.
In clinical trials, except for the clinical investigators and their nurses, all the other Clinical Research Professionals do not perform medical acts. They only work with the study data, the clinical trial organization, data quality control and documentation. Therefore, they don’t need any license to practice in the country. Today most jobs became home-based and are done remotely
Shamisa H. – Iran
Lachance from Montreal
Lebed from Russia
Eyandja – Benin
Gonzalez from Colombia
Touté from Paris
Mathieu from France
Tabataei from Iran
Chountalos – Montreal
Cartamil from Argentina
Kolarov – Bulgaria
Cudjoe from Ghana
Smit from Montreal
Ghamlouche from Syria
Ozcelik from Turkey
Aimable de Québec
Nali – Morocco
Bouslah – Algeria
C. Grand – Boucherville
Stephan from Jordan
Doggui from Pharmascience
Kosher from Montreal
Mefanche from Cameroun
Zamudio from Colombia
Bordeleau from Montreal
Zallif from Morocco
Consultants and Representatives
Clinical Research Advisor
Senior CRA II
Consultant & Mentor
20+ years experience
Data Management Advisor
Ass. Director of Data Management,
Ethica CRO, Montreal
Senior Data Manager
Medical Science Liaison Advisor
SrCRA and MSL
Pharmacovigilance and Drug Safety Advisor
Elite Safety Sciences, USA
PharmD, MBA, MSc, CRRP, PhV
Medical Writing Advisor
Sefika Ozturk, PhD
MSL at Merck
Clinical Trials Management Advisor
Radia Ouelaa, PhD
Clinical Team Manager
Clinical Research Management
Janet Vergara, SrCRA
Ass.Director at Merck
Clinical Research Manager
Clinical Trials Advisor, Trainer and dedicated Mentor
Bahareh Najjar SrCRA
CRA Mentor and Trainer
Team Management Advisor
Anton Lebedev, PhD
Senior Clinical Team Manager at PPD
Regulatory Affairs Advisor and Mentor
IH SrCRA at Merck
Medical Devices Advisor
Monir El Azzouzi,
CEO and Consultant
Easy Medical Device
Medical Writing Advisor and dedicated Mentor
Dr Anand Devasthanam, PhD
Ass. Medical Director
Syneos Health, Boston
Dina Tabatabaei, MA,
CCRP, CRA School Rep
Baltimore, MD, USA.
Daniel Okodan, MSc,
CCRA, CRA at PPD
Taline Sagherian, RD
CCRP, Dubai, UAE
+(971) 50 935 4208
Oluwafemi Ojo, MD, CCRA
Physician, Tawua, Fidji
Alshaimaa Adawy, PhD, MD, CCRA
CRA, MedPace, Munich, Germany
ISSATOU DIALLO, CRA
Afrika at MCT-CRO
Medical Writer, CEO
Peter Zakopcan, CCRP
Sr.PhT in Dubai, UAE
(+971) 50 849 7607
Comprehensive review of Clinical Research studies findings on the CircRNA role in glucose metabolism in Cancer
The requirement of speaking French is blocking the way for foreign-trained candidates, who for family reasons or other considerations decide to settle in Quebec. The article suggest how to issue in advance to be ready for applying immediately after arrival for clinical research roles and avoid delaying your access to these rewarding jobs.
The Global Accessibility Program (GAP) of CRA School is helping close the gap and to build a bridge to clinical research careers
The concept of the PG Clinical Research Certification program is quite unique: It combines very comprehensive regulatory training with 3 remote, part-time monitoring internships to provide the required practical experience, along with unlimited 1-on-1 Placement Assistance Till Hired
To enroll with CRA School Montreal, please fill-in the application form by clicking on the ‘Enroll Today’ button.
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(office closed for quarantine, call)
Information : +1 (514) 534-0273
Support 7/7 : +1 (514) 257-3003
By Skype: CRA School Montreal
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