Cardiovascular CTM – PhD/Recent Grad, Global Trials

Medpace, Inc.; Stirling; On-site; GBP 42,000 - 65,000; Full time

Benefits offered by this job

Competitive compensation

Health, retirement, PTO benefits

WFH flexibility for eligible positions

On-site mentors

Job summary

Medpace, Inc. in Stirling, Scotland is seeking an Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team.

The role targets cardiovascular-related PhDs and/or post-doctoral researchers transitioning into industry and managing clinical studies in collaboration with project coordinators and managers. The position offers an intensive training program, international exposure, and a clear career path in CTM with on-site work and potential opportunities for professional

Qualifications

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

Responsibilities

• Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager.
• 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

English fluency

Presentation skills

International teamwork

Education

PhD in Life Sciences

Job description

Medpace, Inc. in Stirling, Scotland is seeking an Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team.

The role targets cardiovascular-related PhDs and/or post-doctoral researchers transitioning into industry and managing clinical studies in collaboration with project coordinators and managers. The position offers an intensive training program, international exposure, and a clear career path in CTM with on-site work and potential opportunities for professional