Senior Research Nurse

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UT MD Anderson Cancer Center is a leading institution focused on cancer care, research, education, and prevention. Within the Sarcoma Medical Oncology department, faculty and staff are engaged in clinical and translational research focused on improving outcomes for patients with localized and metastatic sarcoma. The department's multidisciplinary team includes medical oncologists, physician-scientists, advanced practice nurses, physician assistants, and research nurses who provide advanced therapies, clinical trial opportunities, and comprehensive patient-centered care.

The Senior Research Nurse is a key contributor to the continued growth of the Sarcoma Clinical Research Program. The Senior Research Nurse manages complex oncology clinical trials, supports patient participation in research, and ensures regulatory compliance and operational excellence. The Senior Research Nurse collaborates across disciplines to advance innovative cancer treatments while maintaining a strong commitment to patient safety, research integrity, and quality outcomes.

The ideal candidate has a Bachelor of Science in Nursing (BSN) with a Master of Science in Nursing (MSN) preferred, a current Texas RN license, and at least three years of oncology clinical research experience. Experience managing Phase I-III clinical trials, informed consent processes, adverse event reporting, and regulatory documentation is highly valued. The successful candidate demonstrates strong knowledge of Good Clinical Practice (GCP), FDA regulations, ICH guidelines, and protocol compliance, along with excellent clinical assessment, communication, organizational, and leadership skills. The ability to manage multiple studies independently in a fast-paced environment while mentoring staff and supporting high-quality patient-centered research is essential for success in this role.

The salary range for this position is Minimum $89,000/annually - Midpoint $111,000/annually - Maximum $133,000/annually

The typical work schedule is days, Monday-Friday, 8 a.m. to 5 p.m.

Why Us?

UT MD Anderson offers the opportunity to contribute to leading-edge sarcoma research while supporting innovative clinical trials that improve survival and quality of life for patients. This role provides professional growth through collaboration with nationally recognized oncology specialists, participation in complex research initiatives, mentorship opportunities, and engagement in a mission-driven environment dedicated to advancing cancer care, research, education, and prevention while supporting 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

Clinical Research Protocol Management

Manage research protocols in collaboration with principal investigators and study sponsors

Assess patient eligibility through interviews and medical record reviews in inpatient and outpatient settings

Coordinate, evaluate, and monitor patient participation throughout clinical trials

Collaborate with multidisciplinary teams to support protocol execution and patient care

Maintain protocol-required documentation within medical records and recruitment logs

Develop and implement patient recruitment strategies

Assist with protocol development, budget planning, and study design

Serve as a liaison between sponsor institutions, pharmaceutical companies, and research teams

Data Collection, Analysis and Reporting

Collect, evaluate, and analyze clinical research data in collaboration with principal investigators

Assess treatment responses, toxicities, and adverse drug reactions

Report findings to principal investigators, Institutional Review Boards, and study sponsors

Prepare protocol summary reports and assist with protocol analysis

Utilize statistical and data management software to support research activities

Design tools that facilitate data collection and analysis

Create user-generated reports and assist with statistical analysis

Develop and maintain research databases while meeting project deadlines

Patient Care & Clinical Trial Support

Perform protocol-specific clinical tasks as required by assigned studies

Educate patients and families regarding treatment management, evaluation, and follow-up during clinical trials

Administer investigational medications following approved nursing procedures and guidelines when required

Collect, label, and process protocol-specific laboratory specimens according to protocol requirements

Order protocol-related tests, consults, and procedures

Obtain pathology slides and tissue blocks as necessary for research protocols

Support safe, effective, and patient-centered participation in clinical trials

Regulatory Compliance & Quality Assurance

Maintain error-free, compliant, and comprehensive protocol management practices

Independently identify and report issues consistent with institutional policies, Code of Federal Regulations, and ICH-GCP guideline

Integrate regulatory policies and procedures into all protocol management activities

Support cross-service research activities as appropriate

Ensure audits consistently demonstrate protocol accuracy, compliance, and data integrity

Develop and conduct random quality reviews of departmental research processes

Support FDA readiness and departmental operational excellence initiatives

Education, Leadership & Professional Development

Educate professional and ancillary staff regarding research protocols through presentations and written guidance

Provide accurate protocol information to multidisciplinary teams, consumers, and professional organizations

Maintain current oncology and data management knowledge through professional development activities

Present clinical trial findings through publications and formal presentations

Develop and evaluate educational materials

Serve as a preceptor, mentor, and resource for staff members

Perform supervisory functions as necessary

Advocate for the clinical research process and associated research roles

EDUCATION

• Required: Graduation from an accredited school of professional nursing.
• Preferred: Bachelor's Degree Nursing and Master's Degree Nursing.

WORK EXPERIENCE

• Required: Two years Registered nurse experience.
• Preferred: Three years of oncology clinical research experience.

LICENSES AND CERTIFICATIONS

• Required: RN - Registered Nurse State of Texas Professional Nursing License (RN).
• Required: BLS - Basic Life Support or
  Cardiopulmonary Resuscitation (CPR).
• Preferred: ACLS - Advanced Cardiac Life Support Certification as required by patient care area.
• Preferred: PALS - Pediatric Advanced Life Support Certification as required by patient care area.
  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.

Additional Information

• Requisition ID: 182207
• Employment Status: Full-Time
• Employee Status: Regular
• Work Week: Days
• Minimum Salary: US Dollar (USD) 89,000
• Midpoint Salary: US Dollar (USD) 111,000
• Maximum Salary : US Dollar (USD) 133,000
• FLSA: exempt and not eligible for overtime pay
• Fund Type: Soft
• Work Location: Hybrid Onsite/Remote
• Pivotal Position: Yes
• Referral Bonus Available?: Yes
• Relocation Assistance Available?: Yes

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