The Clinical Trial Company (CANADA) is recruiting for a OFFICE based Senior Clinical research associate to Monitor studies in Quebec. The ideal candidate will have strong communication skills, both written and oral, in French and English. Candidates should have at least 3 years monitoring experience with either a Pharmaceutical company or CRO.

Candidates should have at least a life science Bachelors degree or an equivalent medical qualification. The successful Clinical Research Associate will ensure that all clinical trial activities meet the ethical and safety requirements of local regulations and ICH GCP.

The CRA will be responsible for:

Site Initiation visits
IRB submission preparation
Routine Monitoring visits
Investigational Drug accountability
Close down visits
Mentoring of trainee CRAs

If you would like to learn more about one of the fastest growing CROs then please send your CV to xx@xxxxxxxxxxxxxxxxxxxxxxx.xxx

It is unlawful to employ a person who does not have permission to live and work in Canada. Unless the advert states otherwise, please ensure you have this permission before applying.