Oncology Data Specialist - CTO

**Job no:** 494074 **Work type:** Clerical **Location:** Oklahoma City **Categories:** Technology/Research **Pay Range:** Targeted annual salary ranges from $34,400 to $43,800, based on experience. **Benefits Eligible:** Yes **Work Schedule:** Monday – Friday, Standard/Fixed Schedule **Travel:** Not required **Position Introduction:** **This is not a remote position and will work 100% onsite.** OU Health Stephenson Cancer Center is Oklahoma’s only National Cancer Institute (NCI)\-Designated Cancer Center, and one of only 74 NCI\-Designated Cancer Centers in the United States. This highly competitive accreditation ensures that our patients receive the highest standard of care and have access to the most advanced cancer treatment options. At the Stephenson Cancer Center, we have an exciting new job opportunity that could be right for you! **Turn data into discovery. Help bring tomorrow’s cancer treatments to life.** Stephenson Cancer Center is seeking a skilled and driven **Oncology Data Specialist** to lead critical data management efforts within the Clinical Trials Office (CTO). In this role, you will serve as a subject matter expert and leader in clinical research data—ensuring accuracy, compliance, and integrity across pharmaceutical and investigator initiated studies. This is an ideal opportunity for a detail oriented professional who thrives in a fast paced oncology research environment and is passionate about advancing innovative cancer therapies through precision data management. Learn more about the Stephenson Cancer Center’s Clinical Trials Office here. **What You’ll Do** **Data Leadership \& Management** * Lead the collection, abstraction, review, and analysis of complex clinical research data * Oversee patient enrollment data and maintain electronic data systems across multiple studies * Assist leadership in prioritizing data volume, timelines, and deliverables **Communication \& Collaboration** * Interpret study protocols and communicate requirements to clinic, chemotherapy, and research staff * Serve as a key liaison between study sites and sponsors regarding data discrepancies and issues * Collaborate with investigators and administrators to support research initiatives and data accuracy **Documentation \& Compliance** * Obtain and verify research source documents from patient records * Ensure all pharmaceutical study documentation meets protocol and regulatory standards * Develop and implement study specific source documents **Data Entry \& Reporting** * Perform and oversee data entry for registration, toxicity, drug, radiation, and pathology data * Prepare advanced study specific reports, queries, and data summaries * Work directly with external monitors to review and resolve data corrections **Additional Responsibilities** * Perform other duties as assigned to support the success of clinical trials and the CTO **Why This Role Matters** Behind every successful clinica