Associate Clinical Trial Manager

About the Role

Medpace is seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will support Project Coordinators and Clinical Trial Managers in performing project management activities. This role is for individuals with a desire to transfer and apply analytical and academic skills in clinical project administration and management.

Key Responsibilities

• Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager.
• Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy.
• Compile and maintain project-specific status reports within the clinical trial management system.
• Interact with the internal project team, Sponsor, study sites, and third-party vendors.
• Provide oversight and quality control of our internal regulatory filing system.
• Provide oversight and management of study supplies.
• Create and maintain project timelines.
• Coordinate project meetings and produce quality minutes.

Requirements & Tech Stack

• PhD in Life Sciences.
• Fluency in English with solid presentation skills.
• Ability to work in a fast-paced dynamic industry within an international team.
• Excellent computer skills (word-processing, databases, Excel, Windows).
• Excellent organizational skills.
• Excellent communication skills.

Qualifications

• Prior experience within the CRO or pharmaceutical industry is not required but will be advantageous.
• Desire and aptitude for an accelerated career path into Clinical Trial Management (CTM).