Associate Clinical Trial Manager (PhD) – Gastrointestinal

Overview

In this role you will join the Clinical Trial Management team to oversee and streamline global trial activities. You will work closely with project coordinators and managers to ensure timely, accurate delivery and documentation. You will gain structured training while applying analytical and academic skills to clinical project administration, with opportunities for rapid progression in CTM within an international 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

• Communicate and collaborate on global study activities with the project coordinator and clinical trial manager
• Ensure timely delivery of recurrent tasks with high accuracy
• Compile and maintain project-specific status reports in the clinical trial management system
• Interact with internal project team, Sponsor, study sites, and third-party vendors
• Provide oversight and quality control of the internal regulatory filing system
• Provide oversight and management of study supplies
• Create and maintain project timelines
• Coordinate project meetings and produce quality minutes

Key requirements

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

• Strong communication
• Collaborative mindset
• Adaptability in a fast-paced environment
• Experience with clinical trial management systems (CTMS)
• Familiarity with regulatory filing processes
• Project coordination and documentation

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