Senior Clinical Project Manager - Advanced Resource Managers

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

Clinical Project Manager II – Clinical Trials

I am currently partnered with a Leading CRO who are looking to enhance their Clincial trial management team based in Canada. Having placed several key hires with this business, I am well placed to advise candidates what this client can do for their careers.

The Project Manager II is responsible for the end-to-end delivery of assigned clinical trials, overseeing study initiation, planning, execution, monitoring, and close-out. This role ensures studies are delivered on time, within budget, and in compliance with SOPs, GCP, regulatory requirements, and sponsor expectations. Acting as the primary sponsor contact, the Project Manager leads cross-functional teams, manages risks, resources, vendors, timelines, and budgets, while ensuring studies remain audit-ready.

Key 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

Requirements

• 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
• Excellent communication, leadership, organizational, and problem-solving skills

Ideal Candidate

A proactive clinical research professional seeking growth within a mid-sized CRO managing complex global, multi-site trials.