Associate Clinical Trial Manager – Renal/GI (PhD)

Medpace, Inc.; Greater London; On-site; GBP 40,000 - 60,000; Full time

Benefits offered by this job

Health benefits

Pension scheme

Paid time off

Job summary

Medpace is seeking a London-based Associate Clinical Trial Manager with renal PhD or post-doctoral research background to join our Clinical Trial Management team. The aCTM will support project coordination and management activities for global studies, applying analytical skills to clinical project administration.

This is an excellent entry point for recent PhD graduates to enter industry, receive solid training, and develop a career in cutting-edge therapeutics within an international

Qualifications

• PhD in Life Sciences is required or strongly preferred.
• Fluency in English with solid presentation skills.
• Ability to work in a fast-paced, international team.
• Prior CRO or pharmaceutical industry experience is not required but advantageous.

Responsibilities

• Communicate and collaborate on global study activities with the project coordinator and CTM.
• Ensure timely delivery of recurrent tasks with high accuracy.
• Compile and maintain project status reports in the CTM system.
• Interact with internal project team, Sponsor, study sites and vendors.
• Provide oversight of regulatory filing system and study supplies.
• Create and maintain project timelines and minutes for meetings.

Skills

English fluency

Presentation skills

International collaboration

Education

PhD in Life Sciences

Job description

Medpace is seeking a London-based Associate Clinical Trial Manager with renal PhD or post-doctoral research background to join our Clinical Trial Management team. The aCTM will support project coordination and management activities for global studies, applying analytical skills to clinical project administration.

This is an excellent entry point for recent PhD graduates to enter industry, receive solid training, and develop a career in cutting-edge therapeutics within an international