Job Details

Pay Range: Targeted annual salary ranges from $34,400 to $43,800, based on experience.Benefits Eligible: TrueWork Schedule: Monday – Friday, Standard/Fixed ScheduleTravel: Not requiredPosition IntroductionOU Health Stephenson Cancer Center is Oklahoma's only National Cancer Institute (NCI)-Designated Cancer Center, and one of only 73 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 DoData Leadership & ManagementLead the collection, abstraction, review, and analysis of complex clinical research dataOversee patient enrollment data and maintain electronic data systems across multiple studiesAssist leadership in prioritizing data volume, timelines, and deliverablesCommunication & CollaborationInterpret study protocols and communicate requirements to clinic, chemotherapy, and research staffServe as a key liaison between study sites and sponsors regarding data discrepancies and issuesCollaborate with investigators and administrators to support research initiatives and data accuracyDocumentation & ComplianceObtain and verify research source documents from patient recordsEnsure all pharmaceutical study documentation meets protocol and regulatory standardsDevelop and implement study specific source documentsData Entry & ReportingPerform and oversee data entry for registration, toxicity, drug, radiation, and pathology dataPrepare advanced study specific reports, queries, and data summariesWork directly with external monitors to review and resolve data correctionsAdditional ResponsibilitiesPerform other duties as assigned to support the success of clinical trials and the CTOWhy This Role MattersBehind every successful clinical trial is high quality, reliable data. As an Oncology Data Specialist, you'll play a pivotal role in ensuring that trial results are accurate, compliant, and impactful—ultimately helping bring life saving treatments to patients faster.View full job description.Required Education and ExperienceHigh School diploma or GED.24 months data entry and quality assurance experience. Advanced degree of proficiency with Microsoft Office Suite, particularly Word and Outlook.Required Certifications and LicensesNoneHiring Contingent Upon a Background CheckYes#J-18808-Ljbffr