Senior Clinical Project Manager

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. If you are interested in this role, please email me on [email protected] or apply via the direct link.

The Project Manager is responsible for the end-to-end delivery of clinical trials, including planning, execution, and close-out. They serve as the primary contact for sponsors and lead cross-functional teams to ensure studies are delivered on time and within budget.

Candidates must have a BSc in a clinical research-related field and over 5 years of industry experience, including 3+ years managing Phase I–III trials. Experience with multi-site trials and knowledge of GCP, ICH, and Canadian regulations are required.

• Google CloudSouhaitée

Relevées dans la description du poste. Confirmez les exigences importantes ci-dessus.

• Clinical Trial Management
• Project Planning
• Budget Management
• Vendor Coordination
• Risk Mitigation
• GCP
• ICH
• FDA Regulations
• Canadian Regulations
• Cross-functional Leadership
• Site Activation
• Audit Readiness

• Science & Research
• Healthcare
• Management & Leadership
• Consulting

Formation minimale

Baccalauréat

Expérience minimale

5+ ans

Langue de l’offre

anglais

Heures de travail

40 heures par semaine

Niveau d’expérience

Mid-Senior level

Mode de candidature

La candidature directe est offerte