Clinical Trial Manager (Associate Director) – London

Overview

In this role you will lead day-to-day operational management of clinical trials in the London office, ensuring compliance with ICH/GCP and applicable regulations. You will act as the primary sponsor contact for operational issues and study deliverables, while guiding cross-functional teams and supervising site quality. The position offers remote flexibility for relevant experience and a strong focus on oncology or other therapeutic areas. You will shape study plans, risk management, and vendor oversight to drive successful trial execution.

Pay / Benefits

• Flexible work environment
• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives

Responsibilities

• Oversee daily operations of trials per contract and regulatory standards
• Serve as sponsor contact for operational issues and deliverables
• Maintain deep knowledge of protocol and therapeutic area
• Provide cross-functional oversight and ensure training for project team
• Review protocols, data checks, analysis plans, and study reports when applicable
• Develop operational project plans and manage risk
• Oversee study vendors
• Supervise site quality and CRAs with monitoring deliverables

Key requirements

• Bachelor’s degree in health or life sciences (advanced degree preferred)
• Minimum 5 years in Clinical Trial Management
• CRO experience preferred
• Experience in Phases 1-4 (2-3 preferred)
• Management of overall project timelines
• Bid defense experience preferred
• Strong leadership skills

• Leadership
• Cross-functional collaboration
• Problem-solving orientation
• ICH/GCP regulatory knowledge
• Trial management and governance
• Vendor management

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