PhD-Ready Associate Clinical Trial Manager

Medpace; Cincinnati (OH); On-site; USD 90,000 - 120,000; Full time

Job summary

Medpace, a Cincinnati-headquartered CRO, seeks an Associate Clinical Trial Manager (aCTM) with PhD and/or post-doctoral experience in Oncology, Hematology, or Radiopharm. This full-time, office-based role supports project managers and coordinators in clinical trial administration, with robust training and growth.

Ideal candidates bring English fluency, strong presentation skills, and the ability to thrive in an international team.

Qualifications

• PhD in Life Sciences or equivalent research experience.
• Fluency in English with solid presentation skills.
• Ability to work in a fast-paced dynamic industry within an international team.
• Prior CRO/pharmaceutical industry experience is advantageous.
• Excellent computer, organizational, and communication skills.

Responsibilities

• Coordinate global study activities with project coordinators and managers.
• Ensure timely delivery of recurrent tasks with high accuracy.
• Maintain project-specific status reports in the trial management system.
• Interact with internal teams, Sponsor, sites, and vendors.
• Oversee and quality-check regulatory filing systems.
• Oversee study supplies and timelines; prepare meeting minutes.

Skills

Project management

Communication

Team collaboration

Education

PhD in Life Sciences

Job description

Medpace, a Cincinnati-headquartered CRO, seeks an Associate Clinical Trial Manager (aCTM) with PhD and/or post-doctoral experience in Oncology, Hematology, or Radiopharm. This full-time, office-based role supports project managers and coordinators in clinical trial administration, with robust training and growth.

Ideal candidates bring English fluency, strong presentation skills, and the ability to thrive in an international team.