Associate Clinical Trial Manager (PhD) – Cardiovascular

Overview

In this role you will support clinical trial management activities within the Stirling-based Clinical Trial Management team. You will work closely with project coordinators and trial managers to ensure timely, accurate delivery of study tasks and to manage project documentation. This is an excellent entry point for recent PhDs to apply analytical and academic skills in a global industry setting. You will undergo intensive training and have an accelerated path into CTM, contributing to cutting-edge therapeutic development in a collaborative 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

• Coordinate global study activities with project teams and sponsors
• Maintain project timelines and status reports in the CTM system
• Provide oversight of regulatory filing systems and study supplies
• Prepare meeting agendas and minutes; support quality control of documentation
• Interact with study sites, vendors, and internal teams to ensure project alignment

Key requirements

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

• clear communication
• team collaboration
• attention to detail
• clinical trial management
• regulatory filing oversight
• project coordination

…