Job Description

Your role will focus on streamlining communication between the study team members, maintaining internal and external Clinical Trial systems and managing documents and study information.

You will:

• Act as the first point of contact for investigational sites, vendors, and multi-functional project teams
• Ensure accurate document management at all times
• Update and maintain (automated) tracking systems and schedules
• Coordinate various activities within clinical research projects
• Organize meetings, prepare agendas and minutes

Required Knowledge, Skills, and Abilities

• BSc or MSc in Life Sciences (or a similar subject), or relevant training and experience
• Administration experience is preferred
• Previous exposure to Clinical Trials is beneficial, although not essential
• Good knowledge of MS Word, Excel and PowerPoint
• Ability to plan, multitask and work in a dynamic team environment
• Excellent communication and collaboration skills