University of Oklahoma

OU Health Stephenson Cancer Center is Oklahoma’s only National Cancer Institute (NCI)-Designated Cancer Center, and one of only 72 NCI-Designated Cancer Centers in the United States.. The Senior Oncology Data Specialist is responsible for leading staff and managing research data, including data collection and entry, and patient enrollment for pharmaceutical and investigator-initiated studies.. Coordinates specimen and tissue submissions with Biorepository staﬀ.. Notiﬁes management and regulatory specialist of all protocol deviations.. 36 months data entry and quality assurance experience in an oncology research environment.

data specialist

<ul><li>Sr. Oncology Data Specialist - Job Number: 240645 </li></ul> Organization : Stephenson Cancer Center Job Location : Oklahoma-Oklahoma City-Health Sciences Center Schedule : Full-time Work Schedule : Monday-Friday 8am-5pm Work Type : Onsite Salary Range : Targeted annual salary from $39,500 to $50,400, based on experience Benefits Provided : Yes Required Attachments : Resume Job Description - - - OU Health Stephenson Cancer Center is Oklahoma’s only National Cancer Institute (NCI)-Designated Cancer Center, and one of only 72 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! The Senior Oncology Data Specialist is responsible for leading staff and managing research data, including data collection and entry, and patient enrollment for pharmaceutical and investigator-initiated studies. Leads the review, abstraction, collection and analysis of data for a specialized program or project. Learn more about the Stephenson Cancer Center’s Clinical Trials Office here. Responsibilities <ul><li> Collects data for patients enrolled in the study and maintains data in electronic data system </li><li> Determines required protocol procedures for clinic, chemo, and surgery and discusses required information with clinic, chemo, and research staﬀ. </li><li> Serves as liaison between site and sponsor regarding data issues and discusses data issues or discrepancies with appropriate staﬀ. </li><li> Obtains research source documents from patient records. </li><li> Veriﬁes pharmaceutical study source documents are correct including required signatures. </li><li> Implements study-speciﬁc source documents. </li><li> Assists with data entry of registration, toxicity, drug, radiation, and pathology data. </li><li> Meets with external monitors to clarify and determine data entry corrections. </li><li> Assist management in prioritization of data volume and timeliness. </li><li> Prepares research charts for clinical and research team. </li><li> Prepares advanced study-speciﬁc reports and queries and discusses with investigators and administrators, including collecting data from other sites. </li><li> Coordinates specimen and tissue submissions with Biorepository staﬀ. </li><li> Monitors for protocol compliance, including dosing, study procedures, tumor measurement, and disease assessment entries. </li><li> Notiﬁes management and regulatory specialist of all protocol deviations. </li><li> Audits study patient documents to identify protocol non-compliance and develops action plans to address deﬁciencies. </li><li> May represent assist Data Management in an external audit. </li><li> May be responsible for providing training or guidance to other Data Managers and staﬀ. </li><li> Performs other duties as needed to successfully fulﬁll the function of the position. </li></ul>Job Requirements - - - Required Education: High School diploma or GED <ul><li> 36 months data entry and quality assurance experience in an oncology research environment. </li></ul>Skills <ul><li> Knowledge of HIPAA </li><li> Working knowledge of HIPAA </li><li> Working knowledge of Common Terminology Criteria for Adverse Events (CTCAE) </li><li> Excellent verbal and written communication skills </li><li> Ability to work as a lead and team member </li><li> Advanced proﬁciency with Microsoft Oﬃce Suite, particularly Word and Outlook </li></ul>Working Conditions <ul><li> Physical: Must be able to sit for prolonged periods of time. </li><li> Environmental: Standard office environment </li></ul> Diversity Statement: The University of Oklahoma is committed to achieving a diverse, equitable, and inclusive university community by recognizing each person's unique contributions, background, and perspectives. The University of Oklahoma strives to cultivate a sense of belonging and emotional support for all, recognizing that fostering an inclusive environment for all is vital in the pursuit of academic and inclusive excellence in all aspects of our institutional mission. Equal Employment Opportunity Statement: The University of Oklahoma, in compliance with all applicable federal and state laws and regulations, does not discriminate based on race, color, national origin, sex, sexual orientation, genetic information, gender identity, gender expression, age, religion, disability, political beliefs, or status as a veteran in any of its policies, practices, or procedures. This includes, but is not limited to, admissions, employment, financial aid, housing, services in educational programs or activities, and health care services that the University operates or provides. Hiring contingent upon a Background Check? : Yes Special Indications : None Job Posting : Mar 7, 2024

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