Associate Clinical Trial Manager, PhD

About the Role

• Full-time, office-based Associate Clinical Trial Manager (aCTM)
• Based in Medpace's Dallas, TX office
• Part of the Clinical Trial Management team, working with Project Coordinators and Clinical Trial Managers on clinical trial management activities.
• Opportunity for recent PhD graduates to enter the industry and develop a career in therapeutic research and development.
• Expect an intensive training period and an aptitude for an accelerated career path into Clinical Trial Management (CTM).

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.
• Desire to transfer and apply analytical and academic skills in clinical project administration and management.