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.

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