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
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