The Clinical Research professional (CRP) Certification and Job Placement Program provides about 115 school hours of 7 theoretical courses (32 chapters) on the FDA (Federal Drug Administration),
Health Canada and EMEA (European Medicines Agency) regulations for clinical trial conduct and monitoring,
continuing Job Placement Coaching & Support till hire and even afterword, and
up to 10 months CRA/CRC "hands-on" working experience in the first in Canada
eCRO.
What distinguishes it from all other programs is that it
includes detailed training on monitoring procedures, plenty of additional practical information and advises, which are not provided in the
usual ICH GCP courses. The program doesn't finish with obtaining of the diploma, but continues with practical internship and coaching with active placement support till hire.
Lectures are
followed by home work tasks and tests and include lot of
practical advises and useful tips for the practical execution of
any CRA or CRC task, experience, that usually takes 1-2 years to acquire.
The program is given either in-class in Montreal, or on-line for all the other candidates, who prefer to save time and money. The on-line program is individual and starts after signature of contract. It is self-paced,
so the students can work whenever they can and advance at their own
speed. To allow francophone candidates to get access to these professions, the in-class program is dispensed in French, but the documentation is in English because interviews and real work are in English, (Min. 6 participants needed)
Bilingual in-class
courses in French start every
3 months if enough participants register. Six to nine months financing is
available for Imm1000 and CSQ holders (received immigrants), as well as a special Accessibility Program for local candidates without revenue
The Internship program allows working as CRA in our eCRO in order to acquire "hands-on" experience while looking for a job (up to 10
months), a major hiring criteria. It gives numerous checklists, templates and practical instructions how to meet all job responsibilities in complicated real life situations. Support by Skype is 7/7.
We provide also corporate training, tailored depending on the specific needs of the companies and professional translation services. clinical trial documentation is translated into more then 12 languages by our ICH GCP trained professionals who know in details the FDA, TCP, FRCQ & EMEA regulations and terminology.
All our interpreters are medical or biomedical professionals, native speakers of the corresponding languages. They are all trained as CRP (CRA/CRC) and work as consultants for us, so they have full professional understanding of what they translate, which removes or reduces substantially the need of back translation and accelerates the process
