PhD to CTM: Associate Clinical Trial Manager (Global)

Medpace; Cincinnati (OH); Presencial; GBP 42.000 - 56.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Flexible work environment

Competitive compensation and benefits

Competitive PTO packages

Structured career paths with growth

Company-sponsored employee events

Employee health and wellness programs

Descripción de la vacante

Medpace is seeking a PhD-level life sciences professional for an Associate Clinical Trial Manager role in the UK. This full-time, office-based position collaborates with Project Coordinators and Clinical Trial Managers to manage global study activities and regulatory processes.

The ideal candidate will have strong English communication and presentation skills, with the ability to work in a fast-paced, international environment. Prior CRO/pharma experience is advantageous but not required.

Formación

• PhD in Life Sciences is required.
• Fluent English with strong presentation skills.
• Experience in a fast-paced international CRO/pharma environment is beneficial but not required.

Responsabilidades

• Communicate and collaborate on global study activities; work closely with the project coordinator and clinical trial manager
• Ensure timely delivery of recurrent tasks with high 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

Conocimientos

English fluency

Presentation skills

Educación

PhD in Life Sciences

Descripción del empleo

Medpace is seeking a PhD-level life sciences professional for an Associate Clinical Trial Manager role in the UK. This full-time, office-based position collaborates with Project Coordinators and Clinical Trial Managers to manage global study activities and regulatory processes.

The ideal candidate will have strong English communication and presentation skills, with the ability to work in a fast-paced, international environment. Prior CRO/pharma experience is advantageous but not required.