Senior Clinical Project Lead – Global Multi-Site Trials

Bilinguallink; Calgary; On-site; CAD 90,000 - 130,000; Full time

Job summary

Bilinguallink is seeking a Clinical Project Manager II – Clinical Trials in Canada to oversee end-to-end delivery of complex studies, including start-up, planning, execution, monitoring and close-out. You will lead cross-functional teams and ensure studies meet budget, timelines and sponsor expectations.

The ideal candidate has a BSc in clinical research, 5+ years industry experience with Phase I–III trials, multi-site management, and strong knowledge of GCP, ICH, FDA and Canadian regulations.

Qualifications

• BSc in a clinical research-related field.
• 5+ years industry experience, including 3+ years managing Phase I–III clinical trials
• Experience managing multi-site clinical trials
• Dermatology or rheumatology trial experience preferred
• Strong knowledge of GCP, ICH, FDA, and Canadian regulations

Responsibilities

• Serve as the main point of contact for sponsors and provide regular study updates
• Lead study planning and execution, including start-up, site activation, vendor coordination, and project deliverables
• Oversee study budgets, timelines, resource allocation, and change orders
• Ensure regulatory compliance, quality standards, and audit readiness
• Monitor recruitment, study progress, and risk mitigation strategies
• Lead and support cross-functional project teams and ensure project-specific training compliance

Skills

Communication skills

Leadership

Organizational skills

Problem solving

Regulatory knowledge

Education

BSc in clinical research field

Job description

Bilinguallink is seeking a Clinical Project Manager II – Clinical Trials in Canada to oversee end-to-end delivery of complex studies, including start-up, planning, execution, monitoring and close-out. You will lead cross-functional teams and ensure studies meet budget, timelines and sponsor expectations.

The ideal candidate has a BSc in clinical research, 5+ years industry experience with Phase I–III trials, multi-site management, and strong knowledge of GCP, ICH, FDA and Canadian regulations.