- Canada
- Full-time · Senior
- 4+ years
Senior Clinical Research Associate responsible for monitoring clinical trials, ensuring data integrity, and managing site visits across multiple countries.
Responsibilities
- Deliver quality monitoring reports
- Maintain expense submissions
- Ensure compliance with ICH GCP/ISO14155
- Monitor sites remotely or onsite
- Plan day-to-day monitoring activities
Requirements
- Undergraduate degree in clinical, science, or health-related field
- Licensed health-care professional (registered nurse)
- Nice to have: global experience
- Nice to have: mentoring experience