PhD-Ready Associate Clinical Trial Manager (Renal)

Medpace; Vlaams-Brabant; On-site; EUR 65,000 - 90,000; Full time

Job summary

Medpace is seeking candidates with Renal related PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Belgium, Leuven Clinical Trial Management team. The aCTM will work with Project Coordinators and Clinical Trial Managers in clinical trial management activities.

This is a fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and

Qualifications

• PhD in Life Sciences.
• 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 with project coordinators and managers.
• Ensure timely delivery of recurrent tasks with high accuracy.
• Compile and maintain project-specific status reports in the CTM system.
• Interact with internal project team, Sponsor, study sites, and vendors.
• Oversee and quality-control our internal regulatory filing system.
• Oversee and manage study supplies.
• Create and maintain project timelines.
• Coordinate project meetings and produce minutes.

Skills

Fluency in English

Education

PhD in Life Sciences

Job description

Medpace is seeking candidates with Renal related PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Belgium, Leuven Clinical Trial Management team. The aCTM will work with Project Coordinators and Clinical Trial Managers in clinical trial management activities.

This is a fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and