Single Sponsor Clinical Project Manager II (Virology) – 1-2 days in Uxbridge (offices moving to London in May26)

Overview

In this role, you will plan, direct, and communicate clinical study timelines for virology trials, coordinating with cross-functional teams to deliver on schedule. You’ll enforce SOP and GCP compliance across studies while selecting sites and vendors and managing budgets. The position involves developing the clinical development strategy and recruitment plans to achieve trial milestones. Based in Uxbridge with an office move to Central London, you’ll contribute to a high-impact, collaborative Clinical Solutions team driving patient progress.

Responsibilities

• Plan, direct, create, and communicate clinical study timelines with cross-functional coordination
• Gather input from regulatory affairs, data management, and clinical operations to build comprehensive study plans
• Ensure consistency of clinical study processes across trials in line with SOP, GCP, and country regulations
• Oversee operational aspects of clinical trials and resolve issues to keep trials on track
• Select sites and vendors, prepare budgets, and ensure studies stay within protocols
• Monitor progress and follow up with team members and line managers on issues
• Implement and prepare the clinical development strategy as outlined by clinical teams
• Develop trial recruitment strategies to ensure participant enrollment

Key requirements

• Bachelor’s degree in a related field
• Minimum of 5 years of experience in clinical project management or related role
• Proven track record of managing clinical trials with adherence to SOP, GCP, and country regulations
• Certification in Clinical Research (e.g., CCRP, CCRA) preferred
• PMI/PMBOK or PMP certification is a plus

• Strong organizational skills
• Excellent communication with cross-functional teams
• Problem-solving abilities
• Knowledge of SOP and GCP
• Experience in site and vendor selection
• Budget preparation and monitoring

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