Associate Clinical Trial Manager (PhD) – Oncology

Overview

In this role you support the Clinical Trial Management team in Stirling, applying academic expertise to clinical project administration. You will collaborate with project coordinators and managers on global study activities, ensuring timely, accurate deliverables and maintaining status reports. You’ll gain solid training in a fast-paced, international setting and contribute to the development of cutting-edge therapeutics. This is a growth path into clinical trial management within a global CRO environment.

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 status reports in the trial management system
• Interact with internal teams, Sponsor, study sites, and vendors
• Oversee internal regulatory filing system quality control
• Oversee study supplies management
• Create and maintain 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
• Prior CRO or pharmaceutical industry experience is advantageous (not required)

• presentation skills
• cross-functional collaboration
• attention to detail
• experience with a clinical trial management system
• project coordination
• regulatory filing oversight

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