1.Review documents in workflow to complete initial indexing.2. Responsible for initial indexing and review of study documentation for Trial Master File (TMF) quality for sponsor and/or CRO studies3. Attend weekly/biweekly meetings with the PMs/clients and discuss project issues and status.4. Check documents in clarification and rejection status for assigned projects.Keep project mappings up to date, coordinate with the study leads for requirement of changes to mappings5. Perform internal reviews of assigned eTMFs for audit readiness.Review internal audit reports and perform corrective actions as required.6. Assist with User Acceptance Testing during product development and release.Work on cross functional teams including Project Management, Business Development, Client Services, Development, and IT on the implementation and management of client projects.7. Gather and provide feedback on features and enhancements that may be needed on an ongoing basis to Development Team.8. Become an expert in the TMF Reference Model and stay current on regulatory changes.9. Become an expert in Trial Interactive features and functionality and work with Director of Clinical Operations, Project Management, and Development to recommend new features. and functionalities to improve the product and reduce manual activities.