Represent Data Management in study team meetings, providing metrics and guidance on data-related issues.
Oversee Data Management activities from study start-up to close-out.
Develop and manage study timelines and ensure the quality and timeliness of data from service providers (e.g., Central Reading Centers, Labs, Medical Coders).
Author key documents, including Data Management Plans, Data Review Guidelines, eCRF Completion Guidelines, and study timelines.
Prepare training materials for Investigator Meetings, internal teams, and site staff.
Maintain all Data Management project documentation in an audit-ready manner.
Support Lead Clinical Programmers in developing and managing Data Transfer Agreements.
Lead regular data review across studies, identifying quality issues, trends, and outliers, and ...