Elevate your clinical project management career with a leading CRO in Canada. This role focuses on overseeing end-to-end clinical trials, ensuring on-time and compliant delivery.

As a Clinical Project Manager II, you will manage the complete lifecycle of clinical trials, driving study initiation through execution and close-out. You'll be responsible for coordinating cross-functional teams, managing budgets and timelines, and ensuring audits align with regulatory compliance. Your expertise in clinical research will be crucial in delivering quality results for sponsors.

Key Responsibilities:
• Serve as the primary contact for sponsors
• Lead planning and execution of clinical studies
• Oversee budgets, timelines, and resource allocation




• Ensure compliance with regulatory standards
• Monitor recruitment and risk mitigation strategies

Requirements:
• BSc in a clinical research-related field
• 5+ years industry experience in clinical trials
• 3+ years managing multi-site trials
• Experience in dermatology or rheumatology preferred
• Solid knowledge of GCP and FDA regulations

Drive successful clinical trials by leveraging your expertise in management and compliance within this impactful role.
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📌 Clinical Project Manager II in Canada (British Columbia)
🏢 Bilinguallink
📍 British Columbia