The Clinical Trial Company (Canada) Ltd. is recruitng for an office-based CRA to monitor studies in Quebec. The ideal condidate will have strong communication skills, both written and oral, in both English and French. Candidates should have at least 3 years monitoring experience with either a Pharmaceutical company or a CRO.
Candidates should have at least a Life Science Bachelor's degree or an equivalent medical qualification. The successful Clinical Research Associate will ensure that all clinical activities meet the ethical and safety requirements of local regulations and ICH GCP.
The CRA will be responsible for:
- Initiation Visits
- Submission Preparation
- Routine Monitoring Visits
- Investigational Drug Accountability
- Close Out 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 the provided email address.
The Clinical Trial Company (Canada) Ltd. (TCTC) is a full service CRO with headquarters in Montreal and the United Kingdom. TCTC operates throughout North America, South America, Europe, India, China, Africa and Australia.