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 anymore in the Academy since May 2020 (legal address only, no admission).
For a FREE 1-hour 1-on-1 Career Consultation on your eligibility, CV adaptation, and Action Plan, suitable for you, contact us by email at email@example.com, by Skype at CRA School Montreal, or by phone from 9:00 AM to 9:00 PM EST (UCT-5), and by Skype chat – till midnight.
By phone: multilingual, 7/7 LIVE Support : +1 (514) 257-3003
WhatsApp: Support 7/7, till 9:00 PM EST : +1 (514) 961-9351
Skype: by chat, 7/7, till 11:30 PM EST @ CRA School Montreal
To call at the right time, use this Time Zone converter
“An investment in knowledge always pays the best interest”
. Benjamin Franklin
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 several are at rather high-level roles today. 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 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. A lot of home-based jobs, excellent for young mothers. Share the news with friends, who face career change, but lack the necessary tools & support, and get a $100 Referral bonus if anyone, whom you informed about us, enrolls someday
N.B.: If you plan moving to Canada, just join us 6-7 months before your flight and arrive JOB READY with a Canadian practical experience from the 3 internships, a Canadian diploma + a network of contacts + unlimited support till hired. This detailed ONLINE program allows to resolve the obstacle of the lacking Canadian experience, to arrive eligible for interviews, and get quickly a job. Share the news <more>
* PATH to Clinical Trials Jobs for international graduates:
Clinical Trials are a great alternative for foreign-trained RN, MDs, BDS, DVM, PharmB/D, PhT & BSc/MSc/PhD degree holders. (No need for recognized diplomas, qualification 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 monitoring internships & 7/7 LIVE Support till hired)
*Most jobs became home-based today. Interesting possibilities for young mothers with babies. Frequent promotions due to the chronic 30% shortage of experienced staff. See more here
* Main obstacle to get into the industry:
The law requires regulatory training AND prior experience (at least from an internship). We provide both + unlimited support till hired. Self-paced study with expected max. duration – up to 2 years. After that exams must be redone.
* What is different in CRP_3.0:
To make students eligible for interviews, in parallel to the regulatory ICH GCP E6(R2) course, 3 remote part-time non-paid monitoring internships on old studies are provided in the Academy, plus:
+ active networking support to get job leads for the “hidden jobs” that are never posted, but filled-in by references,
+ unlimited assistance in the CV adaptation for every role + interview practice and preparation in advance (till hired).
* Who is eligible:
– Candidates worldwide with nursing or any university degrees
– Research assistants, interested to join this rewarding industry
– IMG in career change (MD, DDS, DVM, PharmD, BPharm, RN)
– Clinical Nurses & CRC, looking to jump ships to the industry
* What you will get:
– International PG Diploma of Certified Clinical Research Professional (CRA, IH-CRA, CTA, CRC, DM, PM). All RA roles are covered
– “Hands-on” experience in Canadian/US regulatory environment from 3 monitoring internships, incl. Study Management Software
– Unlimited 7/7 support till midnight EST (UCT-5) from our tutors (NB: we are not a placement company, we assist you till hired)
* Who will profit to enroll:
IMG (RN/MD/DDS/DVM/PharmD/BPharm/MSc/PhD) and any life-sciences graduates worldwide. (No study permit needed. Private studies, not funded by government. Remote 100% ONLINE course, does not provide student’s visa support).
Demo Chapter 12, Informed consent
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Global Accessibility Program (GAP)
In the frame of the Global Accessibility Program (GAP)
an additional regional discount is offered for some
low-income countries in Africa, Asia and Latin America
To enroll, interested candidates must send their CV with
their current home address and their official names as per
their ID to <firstname.lastname@example.org> to verify their eligibility
for the GAP program and to send them a payment invoice.
The concept of our program is totally different. Self-paced
individual (not in a group), starts on the day of enrolling.
Provided worldwide, 100% ONLINE course, with 7/7 direct
contact with a tutor from 9.00 AM till midnight EST (UCT-5).
This flexibility allows to study while working full-time.
The 3 remote part-time monitoring internships are done in
3 Phase II, III & IV studies on metabolic syndrome, LDL-C
and diabetes in the Academy, in parallel to the GCP course
and have a duration of 6 months or more. Support till hired.
* 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?
Do I fit? You probably have hundreds of questions.
For a FREE 1-hour LIVE consultation, just say “Hi” by
Skype to our account “CRA SCHOOL MONTREAL” or
book a time spot 7 days/week here. Reserve 1 hour time.
Get answers to all your questions directly by our expert
Discuss in detail the amazing careers opportunities
in the rewarding and booming clinical trials industry
and what Action Plan would be suitable for you.
To book a FREE 1-hour 1-on-1 Career Consultation
on your eligibility, CV adaptation and an Action Plan,
suitable for you, click here
Well-known fact: Nurses make great Clinical Research Coordinators (CRC) and Clinical Research Associates / Monitors (CRA). They are preferred for CRC & CRA roles, and plenty of other roles too, because they know the principles of ethical clinical practice, the medical terminology, physiology and pathology, diseases and treatments, and how clinics operate.
In Regulatory Affairs (RA), no medical acts are performed, therefore no license to practice in the country is required. Work with data and documents, organization and control of clinical trials. Well paid jobs, no body fluids, no night shifts, no exams. A FAST TRACK road to the profession for foreign trained nurses.
The Accredited Postgraduate Program CRP3.0 provides not only GCP certification, but also practical experience in the clinical trials related tasks, required by law, active support in building a network of contacts with hiring managers, assistance in CV adaptation for every role, plus unlimited interview preparation till hired. The concept is unique and not offered by other training providers.
Contact us for details on how to kick-start your clinical research career. Get 7/7 LIVE Support by an individual tutor till getting the first job in the rewarding clinical trials industry. Proof of qualification required at registration. Foreign diplomas accepted.
SPECIAL DEAL for foreign and Canadian nurses: CAN$ 950.00 / about US$ 755.00
To apply, email your CV to email@example.com to assess your eligibility, and to suggest you a suitable Action Plan.
Become an Affiliate: just share the info with friend
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 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.
Refer us a friend and get a $100 Referral Bonus
Inform friends & colleagues about these highly-paid careers in chronic shortage
of staff, our free monthly Career events, and our Clinical Research PG Diploma
On-boarding 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 & our unique program. We register them
on your name to make sure not to forget to pay you the bonus when they enroll.
Bonuses are paid at the beginning of the month after the candidate enrolled.
The number referrals is unlimited, don’t 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, PPD
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
Clinical Operations Advisor
Anna Leonov, PhD
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
Karima Kezadri, MBA, MSc, CCRP
Regional Rep. for
Maghreb & MENA
New Delhi; India
Dr. Jamil Rashed
Tel: +1 403 465 6900
Tel: +1 306 450 2974
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, Fiji
Alshaimaa Adawy, PhD, MD, CCRA
CRA, MedPace, Munich, Germany
(+256) 756 762 005
ISSATOU DIALLO, CRA
Afrika at MCT-CRO
Medical Writer, CEO
Clinical Trials Monitoring Workshop, Nov.19, Sat, 9:00 AM EST
All you need to know about the clinical trials monitoring visits and CRA role,
presented by Ken Boudrault, SrCRA2 and mentor with 27 years of experence
Meet our Clinical Research Mentors series starts now
Ask all your questions regarding clinical research, monitoring, clinical studies, clinical trials, careers opportunities and how to get-in the industry to Dr Anna Leonov, Clinical Operations Specialist in Syneos Health.
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Getting a clinical research job in Quebec, Canada – challenges and preparation in advance
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.
To enroll with CRA School Montreal, please fill-in the application form by clicking on the ‘Enroll Today’ button.
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(legal address, no admission)
Information : +1 (514) 534-0273
Support 7/7 : +1 (514) 257-3003
By Skype: CRA School Montreal
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