Terumo Medical Corporation

Clinical Research

• Assists with the filing, organization, and ongoing maintenance of essential trial documents within the Trial Master File (TMF), ensuring completeness and accuracy.
• Supports invoice organization and tracking, including filing, reconciliation support, and communication of invoice status to appropriate team members.
• Maintains and update study trackers to support visibility and progress tracking within and across clinical studies.
• Performs quality control (QC) checks on clinical study documentation to verify compliance with internal procedures, regulatory requirements, and Good Clinical Practice (GCP).
• Prepares, assembles, and organizes materials required for the Investigator Site File (ISF), supporting site-level documentation readiness.
• Works on other general clinical operations tasks and ad hoc projects, as needed.

Clinical Research Intern