Perform daily administrative activities to ensure a complete and accurate Trial Master File delivery
Job Summary
Perform daily administrative activities to ensure a complete and accurate Trial Master File delivery.
Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems.
Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
Matching Summary
Perform daily administrative activities to ensure a complete and accurate Trial Master File delivery.
Skills & Requirements
Must-have
Trial Master File (TMF) maintenance
Clinical document handling
Site compliance tracking
Clinical Trial Supplies coordination
Dutch and English language proficiency
Nice-to-have
Effective time management
Organizational skills
Building effective working relationships
Key Requirements
Bachelor's Diploma or equivalent
3-4 years administrative support experience
Prior CTA experience is a strong advantage
Working knowledge of Microsoft Word, Excel and PowerPoint