Clinical Data Coordinator

• Assist in essential data management documentation preparation for various trial stages, including start-up, maintenance, and closeout
• Assist in basic database and edit check testing activities
• Perform data review and query generation
• Perform data entry where required
• Update databases to correct errors
• Assist with generating SAS requests and reviewing report outputs
• Assist with generating data transfers and reviewing transfer outputs
• Assist in activities necessary for finalization and transfer of clinical databases and related project documentation to sponsors
• Ensure approved study documentation is maintained and properly stored in trial master files
• Contribute to continuous improvement of Data Management and the wider organization through information sharing, training, and education
• Promote and advocate for Data Management internally and externally

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