Coordinate study start-up and monitoring activities as a CRA I at ICON Strategic Solutions, with approximately 60% travel required. Use ICH-GCP knowledge to support clinical trials.

Working in a sponsor-dedicated model, you will contribute to ICON’s clinical trial operations function. The role covers study setup, monitoring, status reporting, documentation, and stakeholder collaboration. You will help deliver high-quality outcomes across clinical programmes while supporting patient safety and regulatory compliance.

Key Responsibilities:

- Coordinate study setup and monitoring activities independently
- Complete accurate study status reports and documentation
- Run sponsor-generated queries efficiently and support cost efficiency




- Prepare and review study documentation and feasibility studies
- Maintain relationships with investigators and site staff

Requirements:

- University degree in medicine, science, or equivalent
- Relevant clinical trial monitoring experience
- Knowledge of ICH-GCP guidelines and medical data evaluation
- Excellent written and verbal English communication
- Willingness to travel approximately 60% as required

Bring clinical monitoring, documentation, communication, and ICH-GCP expertise to ICON’s sponsor-dedicated clinical trial programmes.

📌 Study Start Up Clinical Research Associate (Toronto)
🏢 ICON Clinical Research
📍 Toronto