Clinical Trial Manager

Overview

As a Clinical Trial Manager at Medpace in London, you drive day-to-day trial operations within a global CRO framework. You will act as the primary sponsor contact for operational issues and ensure study deliverables meet ICH/GCP standards. You’ll oversee cross-functional teams, risk management, and vendor performance while maintaining deep therapeutic and protocol knowledge. This role offers remote flexibility with relevant experience and opportunities to shape nephrology trials or expand into new areas within a supportive, growth-focused environment.

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 day-to-day project operations per contract and regulatory requirements
• Serve as primary Sponsor contact for operational issues and study deliverables
• Maintain deep knowledge of protocol, therapeutic area, and indication
• Provide cross-functional oversight and ensure project-specific training
• Review study protocol, edit check specs, data analysis plan, and final report when applicable
• Develop operational project plans and manage risk assessment/execution
• Manage study vendor relationships and performance
• Supervise Clinical Research Associates and monitoring deliverables

Key requirements

• Bachelor’s degree in a health or life science-related field; advanced degree preferred
• 5+ years of Clinical Trial Management experience; CRO experience preferred
• Experience in Phases 1-4 (Phases 2-3 preferred)
• Strong leadership and program management skills
• Management of overall project timeline; bid defense experience preferred

• Strong leadership
• Cross-functional collaboration
• Problem-solving
• ICH/GCP knowledge
• Trial management and monitoring
• Vendor management

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