Senior Clinical Research Associate in Quebec City monitoring cardiovascular and respiratory studies, using clinical trial expertise and regulatory knowledge. Approximately 60% travel is required.

At ICON Strategic Solutions, this sponsor-dedicated Senior CRA oversees trial activities and leads technically demanding monitoring work. The position emphasizes protocol adherence, Valuable Clinical Practice, data integrity, and continuous improvement. You will manage multiple sites and projects while guiding site staff and other CRAs.

Key Responsibilities:

- Monitor sites for protocol, regulatory, and GCP compliance
- Conduct site visits and resolve performance issues
- Coordinate accurate, timely data collection and reporting
- Train site staff and other CRAs




- Maintain effective stakeholder and site relationships

Requirements:

- Bachelor’s degree in science or healthcare-related field
- Extensive Clinical Research Associate experience and trial process knowledge
- Ability to manage multiple sites and projects independently
- Expertise in monitoring, data integrity, and site management
- Approximately 60% travel availability

Bring clinical monitoring, compliance, and stakeholder management expertise to cardiovascular and respiratory studies with ICON in Quebec City.

📌 Senior Clinical Research Associate Quebec (Montreal)
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📍 Montreal