Copy of Assistant, Trial Master File

This is a great entry-point for detail-oriented professionals looking to launch a career in clinical research. As a TMF Assistant, you will become the guardian of study integrity, mastering the "gold standard" of clinical documentation.

About the Role:

• Launch Your Career: Perfect for new starters to learn the lifecycle of clinical trials through hands-on TMF management.
• Become a Quality Specialist: Master ALCOA+ principles and SOP compliance to ensure every document is inspection-ready.
• Work Globally: Join an international team, utilizing your English and MS Office skills to coordinate vital project records.
• Dynamic Coordination: Move beyond basic admin by multitasking across diverse projects and attending key team meetings.
• Grow into Leadership: Develop the expertise needed to support audits and CAPA plans, building a strong foundation for future growth.