Clinical Project Manager II

Advanced Resource Managers Ltd; United States; On-site; USD 90,000 - 130,000; Full time

Job summary

Advanced Resource Managers Ltd. is seeking a Clinical Project Manager II to lead end-to-end delivery of dermatology or rheumatology trials across multiple sites in the US.

You will oversee start-up, planning, execution, monitoring, and close-out while ensuring quality, regulatory compliance, and sponsor alignment. Responsibilities include coordinating cross-functional teams, managing budgets and timelines, mitigating risks, and maintaining audit readiness.

Qualifications

• BSc in a clinical research-related field is required.
• 5+ years of industry experience, including 3+ years leading Phase I–III 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.

Responsibilities

• Serve as the main sponsor contact and provide regular study updates.
• Lead study planning, initiation, start-up, site activation, vendor coordination, and deliverables.
• Oversee budgets, timelines, resource allocation, and change orders.
• Ensure regulatory compliance, quality standards, and audit readiness.
• Monitor recruitment, study progress, and risk mitigation.
• Lead and support cross-functional project teams and training compliance.

Skills

Leadership

Communication

Problem-solving

Education

BSc in a clinical research field

Job description

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.

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.