Coordinator, Research Data - GI Medical Oncology

Research Data Coordinator - GI Medical Oncology

The University of Texas MD Anderson Cancer Center is a leading institution focused on cancer care, research, education, and prevention.

The GI Medical Oncology program supports clinical and translational research focused on advancing innovative treatments and improving outcomes for patients with gastrointestinal cancers. The Research Data Coordinator plays an important role in supporting research activities through data collection, documentation, biospecimen management, and patient coordination.

UT MD Anderson is recognized internationally for its commitment to research excellence, patient care, education, and prevention. The Research Data Coordinator works closely with investigators, research staff, clinicians, patients, sponsors, and collaborators to ensure accurate research records, efficient workflows, and successful execution of research initiatives. The Research Data Coordinator contributes directly to the mission of improving patient outcomes through high-quality cancer research.

The ideal candidate will have experience supporting clinical research activities, research data management, biospecimen collection and tracking, quality control processes, and patient coordination. Preferred qualifications include experience with data abstraction, medical terminology, research documentation, multidisciplinary collaboration, effective communication, and workflow improvement.

Minimum $21.15/hour
- Midpoint $26.44/hour
- Maximum $31.73/hour

Work Location:

GI Medical Oncology
- Hybrid
- Houston, TX

The typical work schedule is days

UT MD Anderson offers the opportunity to support groundbreaking cancer research while working alongside leading investigators, clinicians, and research professionals. This role provides meaningful involvement in clinical and translational research initiatives, opportunities for professional growth, and a hybrid work environment that promotes flexibility while contributing to a mission-driven organization focused on improving patient outcomes.

• Employer-paid medical coverage starting day one for employees working 30+ hours/week, plus optional group dental, vision, life, AD&D, and disability insurance.
• Accruals for PTO and Extended Illness Bank, plus paid holidays, wellness, childcare, and other leave options.
• Tuition Assistance Program after six months of service and access to extensive wellness, fitness, and employee resource groups.
• Defined-benefit pension through the Teachers Retirement System, voluntary retirement plans, and employer-paid life and reduced salary protection programs.

• Abstract clinical and research data from Epic, external medical records, laboratory reports, spreadsheets, treatment records, pathology reports, imaging reports, and other source documentation.
• Collect, verify, and enter data into research databases and electronic data capture systems.
• Perform data collection and entry into electronic forms and data portals as required.
• Maintain accurate research databases and ensure data integrity across study-related activities.
• Gather pertinent information through review of medical charts, records, manuscripts, reports, grants, protocols, and supporting documentation.
• Compile research data and prepare ad hoc reports as requested.

• Perform quality assurance and quality control activities to ensure research data completeness, consistency, and accuracy.
• Review and verify database entries to maintain high-quality research records.
• Resolve data discrepancies and respond to investigator, sponsor, collaborator, and regulatory queries.
• Maintain complete, organized, and audit-ready study documentation and research records.
• Ensure compliance with institutional policies, procedures, and research requirements.
• Respond to data-related inquiries while maintaining ongoing data quality standards.
• Develop and maintain systems for processing and tracking research paperwork and documentation.

• Educate and consent patients for research participation and biospecimen collection activities.
• Coordinate, order, collect, document, and track biospecimens and research data from patients.
• Document research activities within the medical record.
• Pend orders for coordinating care teams and follow up to ensure timely completion.
• Request, collect, transport, process, store, ship, and track blood, tissue, and other research specimens.
• Accession materials into the appropriate laboratory system according to study requirements.
• Maintain accurate logs of sample collection, storage, shipment, and disposition.
• Monitor inventory levels and order supplies as needed.
• Maintain an organized inventory room and specimen management processes.

• Request, receive, review, and organize patient records and supporting documentation from outside healthcare institutions.
• Serve as a liaison among patients, investigators,…