Take on a rewarding freelance role as a Senior Clinical Research Associate, focused on conducting essential monitoring activities in Canada. Your expertise will support critical clinical trials and improve patient outcomes. This Senior CRA position requires you to oversee site monitoring, engage in feasibility research, and provide in-house support.

You'll work closely with project teams, manage communication, and be instrumental in the audit process while also preparing regulatory documentation. Bilingual skills in English and French are essential for this role. Key Responsibilities:

- Conduct onsite monitoring visits and report findings
- Review CRFs and verify source documents for accuracy
- Manage communications with site staff
- Support teams during audits and inspections
- Participate in feasibility studies for potential trials Requirements:
- College or university degree in Life Sciences
- Experience with Phase II/III trial monitoring
- Oncology experience is advantageous
- Proficient in MS Office applications
- Valid driver's license and readiness to travel Enhance your clinical research skills while contributing to key medical advancements.

📌 Clinical Research Associate - Freelance Role (Canada)
🏢 PSI CRO
📍 Canada