Associate Clinical Trial Manager (PhD) – Radiopharmaceuticals

Overview

As an Associate Clinical Trial Manager, you will support global clinical trial activities within Medpace’s Clinical Trial Management team, translating academic research skills into practical project administration. You’ll collaborate with project coordinators, trial managers, sponsors, and sites to ensure timely, accurate deliverables while maintaining regulatory oversight. This role offers intensive training, international exposure, and a clear path into Clinical Trial Management. Your work helps advance cutting‑edge therapies through rigorous management and cross‑functional collaboration.

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 coordinators and clinical trial managers
• Ensure timely, accurate delivery of recurring tasks
• Maintain project status reports in the clinical trial management system
• Interact with internal teams, Sponsor, sites, and third‑party vendors
• Oversee internal regulatory filing system quality and compliance
• Manage study supplies and oversee project timelines
• Coordinate project meetings and produce minutes

Key requirements

• PhD in Life Sciences
• Fluency in English with solid presentation skills
• Ability to work in a fast‑paced, international environment
• Experience in CRO or pharmaceutical industry is advantageous but not required

• Strong communication and presentation skills
• Collaborative mindset and team orientation
• Adaptability in a fast‑moving, global setting
• Experience with clinical trial management systems (CTMS)
• Oversight of regulatory filing systems
• Coordination of study supplies and vendor interactions

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