Onsite Research Data Coordinator for Oncology Trials

University of Texas MD Anderson Cancer Center; Houston (TX); On-site; USD 29,000 - 44,000; Full time

Benefits offered by this job

Employer-paid medical coverage (day 1)

Paid time off accruals and holidays

Tuition Assistance Program

Pension and retirement plans

Job summary

The University of Texas MD Anderson Cancer Center's GI Medical Oncology department seeks a Coordinator, Research Data to manage clinical trial data and support studies across oncology protocols. You will collaborate with physicians, research staff, and external partners to ensure data accuracy and protocol compliance.

Responsibilities include building databases, extracting data from EMRs, performing quality checks, and generating reports while promoting trial integrity.

Qualifications

• Bachelor's degree or higher preferred; High School Diploma required.

Responsibilities

• Develop, maintain, and update protocol-specific research databases
• Collect, abstract, and enter patient and study data from electronic health records, treatment records, charts, and external sources
• Perform data review and quality assurance activities to ensure data integrity, accuracy, and completeness
• Generate and maintain protocol-related reports and tracking tools as required
• Assist with implementation and ongoing management of clinical research studies and protocols
• Maintain protocol-related documentation, records, and workflow processes
• Request and obtain medical records and supporting documentation from outside healthcare institutions
• Support specimen collection, tracking, and documentation according to protocol requirements
• Serve as a liaison between patients, physicians, research staff, and external institutions
• Consent patients to designated laboratory protocols and complete documentation within the medical record
• Respond to study-related inquiries and data queries in a timely and professional manner
• Collaborate with physicians, nurses, clinical research coordinators, and other research team members
• Attend departmental, study, and research meetings as required
• Coordinate and assist with monitoring visits and study audits
• Provide cross-coverage and backup support for other research data coordinators as needed
• Perform additional duties as assigned
• Required: High School Diploma or Equivalent
• Preferred: Bachelor's Degree
• Two years Related experience or no experience required with preferred degree.

Skills

Clinical data management

EMR data handling

Data quality assurance

Education

High School Diploma or Equivalent

Bachelor's Degree

Job description

The University of Texas MD Anderson Cancer Center's GI Medical Oncology department seeks a Coordinator, Research Data to manage clinical trial data and support studies across oncology protocols. You will collaborate with physicians, research staff, and external partners to ensure data accuracy and protocol compliance.

Responsibilities include building databases, extracting data from EMRs, performing quality checks, and generating reports while promoting trial integrity.