About this role

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.

At least 18 years of age
Completed at least one year of college and enrolled for Fall 2026
Pursuing a degree in life sciences, health sciences, or related field with interest in clinical research

Clinical Research Intern

Key skills