Associate Clinical Trial Manager – Radiopharmaceuticals

Company: Medpace
Apply for the Associate Clinical Trial Manager – Radiopharmaceuticals
Location: London
Job Description:

Overview

In this role you will join Medpace’s Clinical Trial Management team to support end-to-end trial management for radiopharmaceuticals-related studies. You will collaborate with Project Coordinators, Clinical Trial Managers, and sponsors to drive on-time deliverables and high-quality documentation. The position offers training and a clear path into Clinical Trial Management within an international, research-driven environment. This role focuses on applying your analytical and academic skills to clinical project administration and management, contributing to cutting-edge radiopharmaceutical development.

Pay / Benefits

  • Flexible work environment
  • Competitive compensation and benefits package
  • Competitive PTO packages
  • Structured career paths with opportunities for professional growth
  • Company-sponsored employee appreciation events
  • Employee health and wellness initiatives

Responsibilities

  • Collaborate on global study activities with Project Coordinator and Clinical Trial Manager
  • Ensure timely delivery of recurrent tasks with high accuracy
  • Compile and maintain project-specific status reports in the CTMS
  • Interact with internal teams, Sponsor, study sites, and third-party vendors
  • Oversee internal regulatory filing system for quality and compliance
  • Manage study supplies and oversight
  • Create and maintain project timelines
  • Coordinate project meetings and produce quality minutes

Key requirements

  • PhD or Post-Doc related to Radiopharmaceuticals (nuclear medicine/medical physics/medical imaging/radiation oncology or related)
  • Fluency in English with solid presentation skills
  • Ability to work in a fast-paced dynamic industry within an international team
  • Prior CRO or pharmaceutical industry experience is advantageous but not required
  • strong communication
  • collaboration and teamwork
  • adaptability in a dynamic environment
  • Clinical trial management system (CTMS)
  • regulatory filing oversight
  • radiopharmaceuticals domain knowledge

Posted: September 14th, 2026