Associate Clinical Trial Manager (PhD) – Oncology

Overview

In this role you help drive clinical trial administration within a global team, applying your PhD-level analytical skills to project management. You will work alongside Project Coordinators and Clinical Trial Managers to ensure timely, accurate task delivery and robust study oversight. The position offers structured training and international collaboration, ideal for recent PhD graduates entering industry. You will contribute to regulatory filing oversight, study supplies management, and timeline development, helping advance cutting-edge therapeutics. A strong emphasis is placed on rapid learning, cross-functional teamwork, and a clear path toward CTM leadership.

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 recurrent tasks
• Compile and maintain project-specific status reports in the CTM system
• Interact with internal project team, Sponsor, sites, and third-party vendors
• Oversee and ensure quality of the internal regulatory filing system
• Oversee and manage study supplies
• Create and maintain project timelines
• Coordinate project meetings and produce minutes

Key requirements

• PhD in Life Sciences
• Fluency in English with strong presentation skills
• Ability to work in a fast-paced, international team
• Prior CRO or pharmaceutical industry experience is advantageous but not required

• communication skills
• teamwork and collaboration
• adaptability in a fast-paced environment
• clinical trial management system
• regulatory filing oversight
• project timeline creation

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