PhD-Ready Clinical Trial Manager — Global Oncology Projects

Medpace

Cincinnati (OH)

On-site

GBP 40,000 - 70,000

Full time

14 days+
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Benefits offered by this job

Flexible work environment
Competitive compensation and benefits
Competitive PTO packages
Structured career paths
Company-sponsored employee events
Employee health and wellness
Awards

Job summary

Medpace is seeking an Associate Clinical Trial Manager (aCTM) for a full-time, office-based role to join our Clinical Trial Management team. The candidate will work with Project Coordinators and Clinical Trial Managers on clinical trial activities, leveraging PhD-level knowledge to manage and administer projects.

This entry-level to mid-career opportunity offers intensive training, international exposure, and a clear path toward CTM progression within a leading CRO.

Qualifications

  • PhD in Life Sciences is required.
  • Fluency in English with strong presentation skills.
  • Ability to work in a fast-paced, international team environment.
  • Experience in CROs or pharma is not required but advantageous.

Responsibilities

  • Communicate and collaborate on global study activities with the project coordinator and clinical trial manager.
  • Ensure timely delivery of recurring tasks with high accuracy.
  • Maintain project-specific status reports in the CTM system.
  • Interact with internal project team, Sponsor, study sites, and third-party vendors.
  • Provide oversight of regulatory filing system quality control.
  • Oversee study supplies and logistics.
  • Create and maintain project timelines.
  • Coordinate meetings and produce minutes.

Skills

English fluency
Fast-paced work
International teamwork

Education

PhD in Life Sciences

Job description

Medpace is seeking an Associate Clinical Trial Manager (aCTM) for a full-time, office-based role to join our Clinical Trial Management team. The candidate will work with Project Coordinators and Clinical Trial Managers on clinical trial activities, leveraging PhD-level knowledge to manage and administer projects.

This entry-level to mid-career opportunity offers intensive training, international exposure, and a clear path toward CTM progression within a leading CRO.

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