Associate Clinical Trial Manager (PhD) – Cardiovascular

Overview

In this role you will support the Clinical Trial Management team in London, applying your PhD-level research skills to clinical project administration. You will collaborate with project coordinators, clinical trial managers, sites, and vendors to keep trials on track and compliant. Expect intensive training and an accelerated path into CTM within an international, CRO environment. You will help shape the management of global studies and study materials, contributing to the development of cutting-edge therapeutics.

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 the project team
• Ensure timely, accurate delivery of recurrent tasks
• Maintain project-specific status reports in the CTRM system
• Interact with internal teams, Sponsor, sites, and third-party vendors
• Oversee internal regulatory filing system quality and compliance
• Manage study supplies and oversee logistics
• Create and maintain project timelines
• Coordinate meetings and produce high-quality minutes

Key requirements

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

• strong communication
• cross-functional collaboration
• attention to detail
• clinical trial management
• regulatory filing oversight
• project coordination

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