Senior Clinical Project Manager Regional Municipality

Clinical Project Manager II – Clinical Trials

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.

• 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

• 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

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