05 ott - Bardi
Medpace
Overview
In this full-time, office-based role you join the Clinical Trial Management team as an aCTM, applying your PhD or postdoctoral experience to support global clinical trials.
You will collaborate with Project Coordinators and Clinical Trial Managers to deliver study activities with high accuracy.
The position offers intensive training, international exposure, and a clear path toward leadership in CTM.
This is an opportunity to translate rigorous research skills into practical trial management impact.
Retribuzione / 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
Responsabilità
Collaborate on global study activities with project team and sponsors
Ensure timely delivery of recurrent tasks with high accuracy
Compile and maintain project-specific status reports in the CTM system
Interact with internal project team, Sponsor, study sites, and third-party vendors
Manage and perform 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
Requisiti fondamentali
PhD in Life Sciences
Fluency in English with solid presentation skills
Ability to work in a fast-paced, international team
Prior CRO or pharmaceutical industry experience is advantageous but not required
Strong communication
Team collaboration
Executive presentation??
Clinical trial management
Regulatory filing systems
Project timeline creation
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