Associate Clinical Trial Manager (PhD) – Gastrointestinal

Overview

In this role you will join Medpace’s Clinical Trial Management team to support global trial delivery. You’ll work closely with project coordinators and Clinical Trial Managers to apply analytical and academic skills to clinical project administration. The position offers an intensive training period and a path toward leadership in CTM within an international environment. You’ll help manage timelines, regulatory submissions, and stakeholder communication to advance cutting-edge therapeutics. This role provides a compelling entry point for recent PhD graduates seeking to shape clinical research in a fast-paced setting.

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

• 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 teams, Sponsor, study sites, and third-party vendors
• Provide oversight and quality control of the internal regulatory filing system
• Provide oversight and management of 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 experience in CRO or pharmaceutical industry is advantageous but not required

• strong communication
• cross-functional collaboration
• adaptability
• clinical trial management
• regulatory filing oversight
• project timeline creation

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