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Research Data Specialist - Lymphoma Myeloma
Research Data Specialist - Lymphoma Myeloma
The Research Data Specialist role is a key position within the Lymphoma-Myeloma department of The University of Texas MD Anderson Cancer Center, supporting clinical research operations within the Cancer Medicine Division. The Research Data Specialist works closely with clinical, research, and administrative teams to ensure accurate data management, effective coordination of monitoring activities, and compliance with study protocols that advance patient-focused research.
The University of Texas MD Anderson Cancer Center is a leading institution focused on cancer care, research, education, and prevention. Within UT MD Anderson, the Research Data Specialist contributes to high-impact clinical research efforts by supporting data integrity, regulatory readiness, and operational excellence across lymphoma and myeloma studies. The Research Data Specialist collaborates with multidisciplinary teams to support the mission of eliminating cancer through research-driven discovery and patient-centered care.
The ideal candidate for the Research Data Specialist role demonstrates a strong foundation in research data coordination, monitoring or auditing support, and database development within a clinical research environment. This individual brings relevant education, practical experience in clinical or research settings, and the ability to work with study protocols, data systems, and regulatory requirements while maintaining strong organizational and communication skills.
Minimum $27.64 – Midpoint $34.62 – Maximum $41.59 per hour based on a 40-hour work week. The typical work schedule is days in a hybrid work environment. Work location: Houston, TX
Why Us?
This role directly supports UT MD Anderson’s mission by ensuring the integrity, accuracy, and readiness of clinical research data that drives advancements in lymphoma and myeloma care. The Research Data Specialist benefits from a collaborative environment that values professional growth, learning, and balance while contributing to meaningful research outcomes that impact patients locally and globally.
• 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
Monitoring & Auditing Coordination
• Coordinate and manage the flow of auditors and monitors for assigned clinical trials
• Oversee scheduling and logistics for monitoring and auditing visits
• Ensure completion and documentation of required auditor and monitor checklists
• Facilitate clear and effective communication before, during, and after visits
• Maintain professionalism and attention to detail throughout all visit activities
Research Sample Coordination & Quality Assurance
• Coordinate the collection, handling, and tracking of research samples per study protocols
• Ensure compliance with regulatory and institutional requirements for sample management
• Compile and prepare reports summarizing sample results for study teams and investigators
• Perform quality assurance activities to ensure accuracy and completeness of sample data
• Participate in process improvement initiatives related to sample collection and handling
Database Development & Data Management
• Participate in the development and modification of study databases
• Review study protocols to ensure accurate data fields align with objectives and schedules
• Support incorporation of correct data elements based on protocol requirements
• Seek and complete database development training to maintain current system knowledge
Administrative & Operational Support
• Support study teams with documentation and data readiness activities
• Assist with maintaining organized records for regulatory and study use
• Perform other duties as assigned to support departmental research operations
EDUCATION
- Required: Bachelor's Degree
- Preferred: Master's Degree
WORK EXPERIENCE
- Required: 2 years Research study experience or No experience with preferred degree.
- May substitute required education degree with additional years of equivalent experience.
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
