Associate Clinical Trial Manager, PhD

About the Role

Medpace is seeking candidates with PhDs and/or Post-Doctoral Research experience related to Infectious Disease areas 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 industry. The aCTM will be part of the Clinical Trial Management team, working with Project Coordinators and Clinical Trial Managers on various trial activities.

Key Responsibilities

• Communicate and collaborate on global study activities, working closely with the Project Coordinator and Clinical Trial Manager.
• Ensure timely and accurate delivery of recurrent tasks.
• 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

• Ability to work in a fast-paced dynamic industry within an international team.
• PhD in Life Sciences.
• Expertise related to Infectious Diseases.

Qualifications

• 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.
• Desire and aptitude for an accelerated career path into Clinical Trial Management (CTM).

Note: Compensation range provided ($70,000 - $90,000) and a list of benefits are part of the original text but are not included in this structured output per instructions to focus on factual responsibilities and qualifications.