Elevate your clinical research career as a Senior Clinical Research Associate at ICON Plc in the Greater Toronto Area. Focus on monitoring respiratory and cardiovascular studies while working in a supportive, global team. As a Senior Clinical Research Associate at ICON Solutions, you will be key to managing clinical trial activities and ensuring compliance with study protocols and regulatory standards.

This position requires a deep understanding of clinical trial monitoring, strong organizational skills, and the ability to work independently while mentoring others. You’ll also enjoy a collaborative culture that fosters skilled growth and the development of vital patient treatments. Key Responsibilities:

- Monitor trial sites for protocol adherence and GCP standards




- Conduct site visits to resolve issues and support operations
- Collaborate with teams for accurate data collection
- Train site staff to uphold high clinical standards
- Build relationships with stakeholders to facilitate trials

Requirements:

- Bachelor’s degree in a relevant scientific field
- Extensive CRA experience and understanding of trial processes
- Proven multitasking abilities with organization skills
- Expertise in monitoring and site management
- Excellent communication and interpersonal skills

Drive clinical research excellence by applying your expertise in monitoring and support at ICON Plc in the GTA.

📌 Senior Clinical Research Associate GTA (Toronto)
🏢 ICON Clinical Research
📍 Toronto