Key Skills:
Clinical Data Management (CDM) EDC & Query Management Data Review & Data Cleaning SAE Reconciliation e COA / e PRO e TMF Database Lock Activities ICH-GCP CRO/Vendor Management Responsibilities:
Review and clean clinical trial data. Manage queries and reconcile safety/external data. Support database lock and study deliverables. Maintain e TMF and audit-ready documentation. Coordinate with CROs, vendors, and study teams. Mentor junior team members and ensure data quality. Preferred Background: Clinical Data Manager, Clinical Data Specialist, Clinical Data Coordinator, or Clinical Data Associate with hands-on experience in EDC, query management, and clinical trial data review.