Clinical Trial Manager – UK (London, Stirling) – Neuroscience / Ophthalmology

Overview

As a Clinical Trial Manager at Medpace, you oversee day-to-day operations of CNS-focused clinical studies, ensuring adherence to ICH/GCP and regulations. You serve as the primary sponsor contact, guiding a cross-functional team and overseeing vendors, timelines, and risk. You maintain deep therapeutic area knowledge and contribute to study protocols, analysis plans, and final reports. This role supports Medpace’s mission to accelerate safe, effective therapeutics and offers remote flexibility after probation for relevant experience.

Pay / Benefits

• Flexible work environment
• Competitive compensation and benefits
• Competitive PTO packages
• Structured career paths
• Company-sponsored events
• Employee health and wellness initiatives

Responsibilities

• Lead day-to-day study operations per contract and regulations
• Serve as primary sponsor contact for operational issues and deliverables
• Maintain protocol and therapeutic area knowledge
• Provide cross-functional oversight and ensure project training
• Review input for study protocol, data analysis plan, and final report
• Develop operational project plans and manage risks
• Oversee study vendors and vendor management
• Manage site quality and supervise CRAs and monitoring deliverables

Key requirements

• Bachelor’s degree in health or life science; advanced degree preferred
• Phases 1-4 experience; Phases 2-3 preferred
• Minimum 2 years of Clinical Trial Management experience; CRO experience preferred
• 5+ years of Project Manager/CTM experience at a CRO for remote role
• Strong leadership and project timeline management; bid defense experience preferred

• strong leadership
• effective cross-functional communication
• problem solving
• ICH/GCP compliance
• vendor management
• study protocol review

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