e-CRF Annotation, Data Base Designing. • Extensive Working Knowledge on EDC Systems Inform GTM Clinical trials.• Data Validation, Dynamics Creation, Workflow Creation.• Global Conditions & Edit Check Programming. • Annotate CRFs and configure paper databases and eCRFs, edit checks, and visit schedules.• Perform the necessary quality control steps to confirm if the study is built in accordance with approved specifications.• Resolve and update issues arising from UAT including study database, eCRF and edit checks.• Assess requirements and / or specifications, provide work effort estimates and provide the Study Designer with an estimated turn-around time, based on the approved design specifications.