Etmf Specialist

About the role

Responsible for managing and executing centralized activities supporting global trials with responsible emphasis on clinical documentation. Upload and perform a rigorous quality reviews of electronic documents residing in the eTMF system to ensure they are inspection-ready and are compliant with the ALCOA Plus principles.

What you'll do

• Responsible for managing and executing centralized activities supporting global trials with responsible emphasis on clinical documentation
• Provide immediate feedback for any quality Issue findings
• Interact with regional roles, the study team and other functional areas within BMS to manage document quality
• Review of essential regulatory documentation, including submission of final documents to the eTMF
• Act as single point of contact for the study team for centralized activities related to document management

What you need

• Clinical research
• Documentation
• Quality control
• Communication
• Any graduate