Associate Clinical Trial Manager, PhD

About the Role

Medpace is seeking candidates with PhDs and/or Post-Doctoral Research experience related to CNS/Neuroscience for a full-time, office-based Associate Clinical Trial Manager (aCTM) position in Denver, CO. This role is ideal for recent PhD graduates looking to apply analytical and academic skills in clinical project administration and management within the pharmaceutical industry.

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 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 the 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.
• Expertise related to CNS/Neuroscience.
• Ability to work in a fast-paced dynamic industry within an international team.
• Prior experience within the CRO or pharmaceutical industry is not required but will be advantageous.

Qualifications

• Candidates must have a desire to transfer and apply analytical and academic skills in clinical project administration and management.
• Candidates should show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM).
• Expect an intensive training period.