Join a global leader in clinical research as a Freelance Senior Clinical Research Associate. This role focuses on monitoring and supporting creative 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 audits
Requirements:
• 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 travel
Elevate your clinical research expertise working with a dedicated team on life-changing studies.
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