Data Coordinator I

Job Summary

The Clinical Trials Data Coordinator (Data Coordinator I) will join the Clinical Research Central Office (CRCO) at the University of Wisconsin Carbone Cancer Center (UWCCC) to work on cancer clinical research within one or more Disease-Oriented Teams (DOT).

The Data Coordinator is responsible for completing accurate and timely complex clinical trial data entry and reporting. They also assist in maintaining accurate subject research files. The individual in this role may coordinate sponsor monitoring visits and/or assist with training of staff.

Key Job Responsibilities

• Assists with training of staff
• Performs quality checks
• Collects, abstracts, and interprets subject data from medical records or other source documents. Records and submits subject data to study sponsors, resolves data queries, and verifies accuracy of data
• Maintains research subject charts and ensures all data elements have been accurately collected
• Coordinates and facilitates sponsor monitoring visits
• Provides administrative assistance to a research team
• Assists with data aggregation and reporting for grants, publications, or to satisfy regulatory requirements
• Analyzes protocols during development to determine data capture needs; and contributes to protocol document development
• Assists with Case Report Form (CRF) and related document development