Clinical Data Coordinator (Temporary, Part-Time) - Cancer Center
About The Position
The Clinical Data Coordinator (CDC) will collect, abstract, review, document and monitor data related to clinical research projects. The CDC is responsible for working collaboratively with the Data Manager I, Data Manager II, and Senior Clinical Data Coordinators in the coordination and collection of data for membership, publications, funding, grant submissions, clinical research, and clinical trial accruals. Additional responsibilities include assisting Data Managers with mining, gathering, organizing, and presenting data required for annual reports. The CDC works closely as a liaison for the Clinical Trials Office (CTO) and KUCC Administration. This is a part time temporary position and is not benefits eligible. The University of Kansas Cancer Center (KUCC) is the region's only National Cancer Institute designated comprehensive cancer center where patients gain access to the most promising therapies, cutting-edge clinical trials and world class research.
Requirements
- 4 years of relevant work experience.
- Relevant education may substitute for experience on a year for year basis.
- Experience with technology and data entry.
Nice To Haves
- Oncology experience.
- Experience with database software.
- Data Analysis.
- Computer skills.
- Communication.
- Interpersonal.
- Organization.
- Attention to detail.
- Multi-tasking.
Responsibilities
- Assist Data Managers who are responsible for collecting, managing, and organizing complex enterprise-level data sets for KUCC so that they can be used to create required annual reports, grant submissions, and KUCC member publications.
- Follow Cancer Center Support Grant (CCSG) guidelines for updating the KUCC funding report for NCI-Data Table 1, and Data Table 2, gathering and organizing patient registry data for NCI-Data Table 3, and clinical research data for NCI-Data Table 4.
- Collaborate with the KUCC Members and other stakeholders’ , to ensure data are obtained per grant requirements.
- Communicate regarding data, status and requirements with research staff.
- Assist with the identification and reporting of publications and funding data in accordance with NIH/ NCI reporting guidelines.
- Prepare and provide reports as requested by the Director, Research Systems Operations, Clinical Trials Office.
- Research and resolve data discrepancies; coordinate final annual database closure activities with Data Manager I and participate in audits and process improvement initiatives.
- Successfully manage concurrent priorities and report to Research Systems Operations, Data Manager II.
- Develop a high-level understanding of key KUCC business processes, workflows, and information flows.
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What This Job Offers
Job Type
Part-time
Career Level
Entry Level
Education Level
No Education Listed
