Clinical trial monitoring and site relationship management define this Canada-based Clinical Research Associate II chance with Novotech. Protect participants and verify accurate trial data.

As a Clinical Research Associate II, you will connect Investigational Sites, Novotech, and Sponsors throughout clinical trials. The work includes ICH GCP monitoring, regulatory requirements, site relationships, recruitment, and clinical trial management systems. You will support study execution across monitoring visit types and trial phases.

Key Responsibilities:

- Build relationships with investigators and site trial personnel
- Monitor sites onsite or remotely under the Clinical Monitoring Plan
- Protect participants and review consent, eligibility, compliance, and safety




- Verify CRF data and resolve queries within study timelines
- Maintain trial systems and keep the Trial Master File current

Requirements:

- Graduate degree in clinical or life sciences-related field
- Approximately one to two years of CRA experience
- Good time management and attention to detail
- Computer literacy and ability to work well in teams
- Fluency in French is highly prioritized

Apply clinical research, ICH GCP monitoring, and site management expertise to support accurate, compliant trials across Canada.

📌 Clinical Research Associate II Canada
🏢 Novotech CRO
📍 Canada