Clinical Project Manager II
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What you'll do
- 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
What they're looking for
- 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 is a must
- Strong knowledge of GCP, ICH, FDA, and Canadian regulations
- Excellent communication, leadership, organizational, and problem-solving skills
Summarised by NextRaise from the employer’s description, which follows in full below.
Full description from employer
Clinical Project Manager II - Clinical Trials
I am currently partnered with a Leading CRO who are looking to enhance their clinical trial management team based in Canada. Having placed several key hires with this business, I am well placed to advise candidates on 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 is a must
* 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 vik.patel@arm-talent.com or apply via the direct link.
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Disclaimer:
This vacancy is being advertised by either Advanced Resource Managers Limited, Advanced Resource Managers IT Limited or Advanced Resource Managers Engineering Limited ("ARM"). ARM is a specialist talent acquisition and management consultancy. We provide technical contingency recruitment and a portfolio of more complex resource solutions. Our specialist recruitment divisions cover the entire technical arena, including some of the most economically and strategically important industries in the UK and the world today. We will never send your CV without your permission.
Company
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