French-fluent Clinical Research Associate work in Quebec, monitoring Phase I-IV trials and device studies through onsite and remote visits.

Premier Research seeks a Clinical Research Associate II or Senior Clinical Research Associate with four-plus years of onsite monitoring experience. You will support oncology, pediatrics, rare disease, and other clinical studies while protecting data integrity and patient safety. The work includes investigative-site communication, trial documentation, and visit management.

Key Responsibilities:

- Conduct qualification, initiation, monitoring, management, and closeout visits
- Verify clinical data validity, correctness, completeness, and integrity
- Manage site queries and support Trial Master File activities




- Identify risks and investigative-site retraining opportunities
- Plan visits, trip reports, and study deliverables

Requirements:

- Undergraduate degree or international equivalent
- Four-plus years of onsite clinical research monitoring experience
- French fluency and residence in Quebec
- Ability to complete eight to ten monitoring visits monthly
- Valid driver’s license and passport as required

Apply clinical monitoring, French fluency, and site-management expertise across patient-focused studies with Premier Research in Quebec.

📌 Senior Clinical Research Associate Quebec (Quebec City)
🏢 Premier Research Group
📍 Quebec City