Position Introduction

OU 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.

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