Coordinator, Research Data - Lymphoma Myeloma

Research Data Coordinator - Lymphoma Myeloma

The University of Texas MD Anderson Cancer Center is a leading institution focused on cancer care, research, education, and prevention. The Research Data Coordinator supports the collection, maintenance, tracking, and reporting of clinical research data while helping ensure protocol compliance, data integrity, and operational efficiency across research studies. The Research Data Coordinator works closely with research nurses, physician investigators, sponsors, auditors, and monitors to support clinical trial activities and research operations.

UT MD Anderson is committed to advancing cancer research through innovative clinical trials and high-quality research programs. The Research Data Coordinator plays an essential role in maintaining accurate study documentation, supporting protocol execution, coordinating research data and sample activities, and facilitating communication among multiple stakeholders involved in clinical research.

The ideal candidate will possess strong organizational, communication, and data management skills with the ability to support clinical research activities, coordinate across departments, manage study documentation, and maintain compliance with research protocols. Candidates should be comfortable working independently in a remote environment while interacting professionally with investigators, sponsors, auditors, monitors, and research staff.

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

Work Location: Remote (Houston, Texas)

The typical work schedule is days

Why Us?

This position directly supports UT MD Anderson's mission to eliminate cancer by contributing to the successful execution of clinical research studies. The role offers the opportunity to work collaboratively with research professionals, investigators, and sponsors while building expertise in clinical trials, data management, regulatory compliance, quality assurance, and research operations in a remote work environment that supports professional growth and work-life balance.

• 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.

Responsibilities

• Monitor toxicity and response to study agents and report findings to the appropriate source, including research nurses, physician investigators, and sponsors as requested.
• Review research records and communicate findings to the appropriate source, including research nurses, physician investigators, and sponsors as requested.
• Develop and maintain tracking systems to control protocol activities, patient visits, research samples, and study documents.
• Enter required protocol data into designated data control systems in accordance with research requirements.
• Assist with preparation and maintenance of protocol data reports.
• Support Physician Investigators with clinical trial presentations, publications, and assigned research projects.
• Assist in the management of research samples and research data as needed.
• Collaborate with multiple departments to collect research data and research samples required for protocol completion.
• Communicate effectively with internal departments to prevent protocol deviations and protocol violations.
• Participate in departmental Quality Assurance rotation activities and assigned quality assurance responsibilities.
• Manage the flow of auditors and monitors for assigned clinical trials.
• Oversee monitor visits and ensure completion of all required auditor and monitor checklists.
• Coordinate appointments and logistics for auditors and monitors as needed.
• Demonstrate a high level of professionalism and organizational skills while supporting auditor and monitor activities.
• Perform other duties as assigned.

EDUCATION

• Required: High School Diploma or Equivalent
• Preferred: Bachelor's Degree

WORK EXPERIENCE

• Required: Two years related experience or no experience required with preferred degree.

The University of Texas MD Anderson Cancer Center offers excellent benefits, including medical, dental, paid time off, retirement, tuition benefits, educational opportunities, and individual and team recognition.

This position may be responsible for maintaining the security and integrity of critical infrastructure, as defined in Section 113.001(2) of the Texas Business and Commerce Code and therefore may require routine reviews and screening. The ability to satisfy and maintain all requirements necessary to ensure the continued security and integrity of such infrastructure is a condition of hire and continued employment.

It is the policy of The University of Texas MD Anderson Cancer Center to provide equal employment opportunity without regard to race, color, religion, age, national origin, sex, gender, sexual orientation, gender identity/expression, disability, protected veteran status, genetic information, or any other basis protected by institutional policy or by federal, state, or local laws unless such distinction is required by law.http://www.mdanderson.org/about-us/legal-and-policy/legal-statements/eeo-affirmative-action.html

Additional Information

• Requisition ID: 182372
• Employment Status: Full-Time
• Employee Status: Regular
• Work Week: Days
• Minimum Salary: US Dollar (USD) 44,000
• Midpoint Salary: US Dollar (USD) 55,000
• Maximum Salary : US Dollar (USD) 66,000
• FLSA: non-exempt and eligible for overtime pay
• Fund Type: Soft
• Work Location: Remote (within Texas only)
• Pivotal Position: No
• Referral Bonus Available?: No
• Relocation Assistance Available?: No

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