Monitor oncology and gastroenterology trials with PSI from Canada’s West Coast, applying independent site monitoring and clinical research expertise.

As a Clinical Research Associate, you will monitor Phase I–III studies across different therapeutic indications. You will communicate with sponsors, project teams, investigators, and sites while maintaining quality, compliance, and data integrity. The work includes site visits, recruitment oversight, and study documentation.

Key Responsibilities:

- Prepare, conduct, and report site monitoring visits
- Maintain communication and relationships with study site staff
- Verify source data and resolve site data queries
- Manage investigational products, supplies, and essential documents
- Support audits, training, submissions, and tracking systems

Requirements:

- College or university degree in Life Sciences
- Five or more years of independent onsite monitoring
- Independent Phase I–III oncology trial monitoring experience
- Independent gastroenterology IBD trial monitoring experience
- Canada West Coast location and ability to travel 75%

Apply independent monitoring, oncology, and gastroenterology expertise to support compliant clinical studies with PSI.

📌 Clinical Research Associate Oncology (Calgary)
🏢 PSI CRO
📍 Calgary