Oncology Clinical Trial Manager - Flexible Growth Path

Medpace; Stirling; On-site; GBP 30,000 - 50,000; Full time

Benefits offered by this job

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

Job summary

Medpace is seeking a full-time Associate Clinical Trial Manager (aCTM) in Stirling, United Kingdom. Ideal candidates hold Oncology-related PhDs and are eager to develop their career in clinical trial management. Responsibilities include collaboration on global studies, oversight of project timelines, and maintaining regulatory files. The role offers a flexible work environment, competitive compensation, structured career paths, and opportunities for professional growth. Training will be provided to facilitate an accelerated career path in the research of cutting-edge therapeutics.

Qualifications

• PhD in Life Sciences required for the position.
• Fluency in English with solid presentation skills.
• Ability to work in a fast-paced dynamic industry within an international team.

Responsibilities

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

Skills

Analytical skills

Collaboration

Communication

Presentation skills

Education

PhD in Life Sciences

Job description

Medpace is seeking a full-time Associate Clinical Trial Manager (aCTM) in Stirling, United Kingdom. Ideal candidates hold Oncology-related PhDs and are eager to develop their career in clinical trial management. Responsibilities include collaboration on global studies, oversight of project timelines, and maintaining regulatory files. The role offers a flexible work environment, competitive compensation, structured career paths, and opportunities for professional growth. Training will be provided to facilitate an accelerated career path in the research of cutting-edge therapeutics.