Oncology Data Specialist - CTO
About The Position
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. Behind 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.
Requirements
- High School diploma or GED
- 24 months data entry and quality assurance experience
- Advanced degree of proficiency with Microsoft Office Suite, particularly Word and Outlook
Nice To Haves
- Proficiency with Microsoft Office (Excel, Word, Outlook)
- Attention to detail and data accuracy
- Excellent written and verbal communication skills
- Ability to work independently and collaboratively
- Problem-solving skills
- Knowledge of HIPAA guidelines
Responsibilities
- 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
- 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
- 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
- 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
- Perform other duties as assigned to support the success of clinical trials and the CTO
Benefits
- Benefits Eligible: Yes
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED
