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 unlimited CRA/CRC "hands-on" working experience in
eCRO environment.
What distinguishes it from all other programs is the detailed training on monitoring procedures and the additional practical advises and useful tips, not provided in the
usual 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 internship for practical execution of
all major CRA or CRC tasks to acquire experience, that usually takes 1-2 years to acquire.
The program is given either in-class in Montreal (min. 6 participants needed), or on-line for the candidates, who prefer to save time and money or live elsewhere. The on-line program is individual and self-paced,
so the students can work 7/7 whenever they can and advance at their own
speed. The in-class program is dispensed in French to allow francophone candidates to get access to these professions, but the documentation is in English because interviews and real work are in English.
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.
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
We provide also 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, FRSQ & EMEA regulations and terminology. All our interpreters are medical or biomedical professionals, native speakers of the corresponding languages. This removes or reduces substantially the need of back translation and accelerates the process
