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Candidates local or willing to relocate to the Cincinnati Tri-State are highly preferred. JOB RESPONSIBILITIES * Database Management- Designs, develops, and maintains databases in accord with established data management plans and GCDMP guidelines. Develops programs using statistical analysis system (SAS) language or other statistical software for the development of analytical datasets and reports. Develops rigorous quality control and quality assurance programs to perform data validation for data generated from clinical research studies and other databases to assure agreed upon data quality. Creates and follows standardized data quality processes to ensure reproducibility and increase efficiencies. May identify inconsistencies and discrepancies in data and takes the necessary steps to correct. * Data Systems- Collaborate with team members from various departments on the design, documentation, testing and implementation of clinical data management research systems studies. Develop systems for organizing data to analyze, identify and report trends. Design and maintain clinical databases. Designs and/or reviews Case Report Forms (CRFs). Develops process for incorporating laboratory and other external data. Develop, implement and maintain data management plans for clinical research studies programs of broad scope and complexity. Create and maintain detailed data dictionaries and data management documentation. * Quality Assurance- Participate in protocol reviews and identify critical data items required for analysis and reporting. Consult with senior peers on non-routine projects to learn through experience. Ensure accurate project-related databases through the timely generation of logic statements, querying of data, edit checks, resolution of inaccuracies and auditing of databases in accord with GCDM practices. * Reporting and Documentation- May create and maintain detailed data dictionaries and data management operation manuals for research studies. Creates summary tables, graphs, and listings for study coordination efforts via programming. Maintains clear documentation of all processes and procedures followed to produce all outputs. JOB QUALIFICATIONS * Bachelor's degree in a related field * 3+ years of work experience in a related job discipline * Experience in health care clinical trials research is highly preferred * Experience communicating and presenting data insights is preferred * Experience using SAS or R is preferred Primary Location Burnet Campus Schedule Full time Shift Day (United States of America) Department Cardiothoracic Surgery Employee Status Regular FTE 1 Weekly Hours 40 *Expected Starting Pay Range *Annualized pay may vary based on FTE status$61,401.60 - $78,291.20 About Us At Cincinnati Children's, we come to work with one goal: to make children's health better. We believe in a holistic team approach, both in caring for patients and their families, and in advancing science and discovery. We strive to do better and find energy and inspiration in our shared purpose. If you want to be the best you can be, you can do it at Cincinnati Children's. Cincinnati Children's is: * Recognized by U.S. News & World Report as atop 10 best Children's Hospitals in the nation for more than 15 years * Consistently among the top 3 Children's Hospitals for National Institutes of Health (NIH)Funding * Recognized as one of America's Best Large Employers (2025), America's Best Employers for New Grads (2025) * One of the nation'sAmerica's Mo Apply here: https://www.aplitrak.com/?adid=YmJnZW5lcmljLjM3Mjg4LjEwNTA4QGNpbmNpbm5hdGljaGlsZHJlbnNjb21wLmFwbGl0cmFrLmNvbQ