Full-Time

Senior Oncology Data Specialist

Cto

Posted on 10/4/2025

University of Oklahoma

University of Oklahoma

No salary listed

Oklahoma City, OK, USA

In Person

Category
Lab & Research (1)
Requirements
  • 36 months data entry and quality assurance experience in an oncology research environment
  • High School diploma or GED
Responsibilities
  • Collects data for patients enrolled in the study and maintains data in electronic data system
  • Determines required protocol procedures for clinic, chemo, and surgery and discusses required information with clinic, chemo, and research staff. Serves as liaison between site and sponsor regarding data issues and discusses data issues or discrepancies with appropriate staff.
  • Obtains research source documents from patient records. Verifies pharmaceutical study source documents are correct including required signatures. Implements study-specific source documents.
  • Assists with data entry of registration, toxicity, drug, radiation, and pathology data. Meets with external monitors to clarify and determine data entry corrections. Assist management in prioritization of data volume and timeliness.
  • Prepares research charts for clinical and research team. Prepares advanced study-specific reports and queries and discusses with investigators and administrators, including collecting data from other sites. Coordinates specimen and tissue submissions with Biorepository staff.
  • Monitors for protocol compliance, including dosing, study procedures, tumor measurement, and disease assessment entries. Notifies management and regulatory specialist of all protocol deviations. Audits study patient documents to identify protocol non-compliance and develops action plans to address deficiencies. May represent assist Data Management in an external audit.
  • May be responsible for providing training or guidance to other Data Managers and staff. Performs other duties as needed to successfully fulfill the function of the position.
Desired Qualifications
  • Working knowledge of HIPAA
  • Working knowledge of Common Terminology Criteria for Adverse Events (CTCAE)
  • Excellent verbal and written communication skills
  • Ability to work as a lead and team member
  • Advanced proficiency with Microsoft Office Suite, particularly Word and Outlook
University of Oklahoma

University of Oklahoma

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