Join a global leader in clinical research as a Freelance Senior Clinical Research Associate. This role focuses on monitoring and supporting cutting-edge medical studies across Canada.We're seeking an experienced CRA to conduct onsite monitoring visits and ensure compliance with study protocols. You will play a critical role in site management and communication, supporting both the regulatory team and internal project groups.

This position is well-suited for candidates with expertise in Phase II and III monitoring.Key Responsibilities:

- Conduct and report site initiation, monitoring, and close-out visits• Perform CRF review and source document verification• Manage site communications effectively• Act as a liaison for support services and vendors• Participate in feasibility research and auditsRequirements:
- Degree in Life Sciences or equivalent experience• Proven experience in Phase II and/or III monitoring• Experience in Oncology is an asset• Bilingual proficiency in English and French• Valid driver’s license and willingness to travelElevate your clinical research expertise working with a dedicated team on life-changing studies.

📌 Freelance Senior Clinical Research Associate (Toronto)
🏢 PSI CRO
📍 Toronto