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 skilled seeking growth within a mid-sized CRO managing complex global, multi-site trials.

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📌 Senior Clinical Project Manager - etobicoke (Ontario)
🏢 Bilinguallink
📍 Ontario