Monitor cardiovascular and respiratory clinical trials as a Senior CRA with ICON Plc in Quebec City. Apply GCP knowledge and site management expertise. This sponsor-dedicated position focuses on overseeing trial activities according to protocols, regulations, and industry standards. You will conduct site visits, assess performance, support execution, and address issues requiring technical depth. Robust communication, organization, and problem-solving skills support work across sites, projects, and stakeholders.

Key Responsibilities
- Assess site performance during clinical trial visits
- Resolve site issues and support successful execution
- Ensure adherence to protocols and regulatory requirements




- Collaborate on clinical data collection and reporting
- Guide staff toward high conduct standards

Requirements:
- Relevant scientific or healthcare bachelor’s degree
- Strong clinical trial monitoring and regulatory understanding
- Experience managing multiple sites and projects
- Proficiency with clinical trial software and tools
- Excellent communication and stakeholder management skills Use site monitoring, data integrity, and compliance expertise to support ICON’s cardiovascular and respiratory clinical research in Quebec.

📌 Clinical Trial Monitor Cardiovascular Respiratory (Montreal)
🏢 KCR Placement
📍 Montreal