Associate Clinical Trial Manager (PhD) – Renal / Gastrointestinal

Overview

In this role you will join Medpace’s London Clinical Trial Management team to oversee and support global clinical trial activities. You will work closely with project coordinators and clinical trial managers to ensure timely, accurate delivery and robust project governance. You’ll engage with sponsors, sites, and vendors, while overseeing regulatory filing quality and study supplies. This role offers training, international exposure, and a clear path into clinical trial management within a mission-driven CRO.

Pay / Benefits

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

Responsibilities

• Communicate and collaborate on global study activities with project coordinators and clinical trial managers
• Ensure timely delivery of recurrent tasks with high accuracy
• Compile and maintain project-specific status reports in the CTM system
• Interact with internal project team, Sponsor, study sites, and third-party vendors
• Oversee and quality-control internal regulatory filing system
• Oversee and manage study supplies
• Create and maintain project timelines
• Coordinate project meetings and produce quality minutes

Key requirements

• PhD in Life Sciences
• Fluency in English with solid presentation skills
• Ability to work in a fast-paced, international team
• Prior CRO or pharmaceutical industry experience is not required but advantageous

• strong communication
• collaboration across cross-functional teams
• presentation skills
• clinical trial management system
• regulatory filing oversight
• project coordination and timelines

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