- Pointe-Claire, Quebec, Canada +1 more
- On-site
- Full-time · Entry
- 1+ years
Support the execution of clinical studies by performing administrative and clinical responsibilities at a research site.
Locations (2)
- Pointe-Claire, Quebec, Canada
- Mirabel, Quebec, Canada
Responsibilities
- Coordinate study visits and participant safety
- Perform clinical procedures such as vitals, ECG, phlebotomy
- Recruit, screen, and enroll participants
- Document study data and regulatory records
- Prepare for monitoring visits, audits, and inspections
Requirements
- Nice to have: Clinical research coordination
- Nice to have: Informed consent
- Nice to have: Recruitment
- Nice to have: ICF
- Nice to have: Health Canada regulations