Description

*About Us* Here at Baylor Scott & White Health we promote the well-being of all individuals, families, and communities. Baylor Scott and White is the largest not-for-profit healthcare system in Texas that empowers you to live well. Our Core Values are: * We serve faithfully by doing what's right with a joyful heart. * We never settle by constantly striving for better. * We are in it together by supporting one another and those we serve. * We make an impact by taking initiative and delivering exceptional experience. *Benefits* Our benefits are designed to help you live well no matter where you are on your journey. For full details on coverage and eligibility, visit the Baylor Scott & White Benefits Hub to explore our offerings, which may include: * Eligibility on day 1 for all benefits * Dollar-for-dollar 401(k) match, up to 5% * Debt-free tuition assistance, offering access to many no-cost and low-cost degrees, certificates and more * Immediate access to time off benefits At Baylor Scott & White Health, your well-being is our top priority. Note: Benefits may vary based on position type and/or level *Job Summary* The Research Data Coordinator finds, obtains, and integrates data from research and clinical sources. They prepare and upload data to public repositories. They develop and troubleshoot study-specific eCRFs and events using clinical trial management software. They manage clinical trial paper data sources like eCRFs and study protocols. They perform data entry and validation. They educate others in proper clinical trial data management, entry, and validation procedures. This role will help support the Texas Immuno-Oncology Biorepository (TIOB), which was created to collect, catalog and store samples of biological material along with data collection in an effort to improve our understanding of cancer. *Essential Functions of the Role* * Locates, procures and integrates data. * Develops and troubleshoots study-specific eCRFs and events using clinical trial management software. * Manages clinical trial paper data sources. * Educates others in proper clinical trial data management, entry and validation procedures. * Performs data entry and validation. *Key Success Factors* * Must be detail oriented. * Must be well organized. * Ability to locate, collate and integrate data from diverse sources. * Ability to effectively utilize common bioinformatics, office and clinical trial software. * Ability to interact with research and clinical personnel. * Ability to adjust to rapidly changing requirements. * Ability to teach and present. * Knowledge of NIH, HIPAA and FDA regulations surrounding data management. *Belonging Statement* We believe that all people should feel welcomed, valued and supported, and that our workforce should be reflective of the communities we serve. *QUALIFICATIONS* * EDUCATION - Associate's * EXPERIENCE - Less than 1 Year of Experience