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
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