Research Nurse

Research NurseThe Division of Clinical Research provides infrastructure support for all aspects of clinical research.The primary purpose of the Research Nurse position is to provide and coordinate independent, advanced research and protocol-related clinical aspects of investigational trials in collaboration with the multidisciplinary team and external sponsors to achieve quality clinical trials outcomes within the Harris Health/LBJ Research Program. Scope of position is defined by the Nurse Practice Act of the State of Texas and requires adherence to the policies and procedures of the institution.The ideal candidate will have oncology care experience, and research experience. The successful candidate will demonstrate strong organizational skills, the ability to work independently, and experience coordinating complex clinical activities within a research environment.Minimum $37.26/hour – Midpoint $46.63/hour – Maximum $56.01/hour The typical work schedule is Hybrid. Why Us? Join UT MD Anderson and contribute to advancing groundbreaking clinical research that improves outcomes for patients with cancer. This role offers the opportunity to work with multidisciplinary teams, innovative treatment protocols, and leading clinical research programs while supporting professional growth, work-life balance, and meaningful patient impact.Responsibilities Coordination of CareManage resources available to facilitate the informed consent process across treatment, interventional, and non-interventional clinical trialsVerify patient eligibility and provide feedback to physicians and multidisciplinary teams regarding required screening activities and scheduling time constraintsSchedule patient tests and keep patients informed of test results and study-related activitiesServe as a liaison between patients, physicians, and research staff to coordinate research studiesTrack protocol-related laboratory work, patient responses, and research testing requirementsMonitor patients enrolled in chemotherapy, immunotherapy, and cell therapy treatment trialsCommunicate dose delays and dose reductions based on hematological and clinical criteria to treatment teamsIdentify and address educational, emotional, and psychosocial needs of patients and their families participating in clinical trialsUtilize the OneConnect system to ensure research charges are appropriately documented and billing to sponsored study accounts is accurateProtocol ManagementMaintain expert knowledge of adverse events and applicable reporting policies and proceduresPrepare and review data required for monitoring visits, audits, and safety summariesLead patient update calls with study sponsorsCollect and develop critical information for protocol submissions and protocol revisionsCoordinate FDA-related documentation, including collection, de-identification, and submission of serious adverse event documentation to sponsors and oversight organizationsCollaborate with the Investigational New Drug Office, Clinical Research Organizations, and other regulatory oversight groups as requiredMaintain communication with participating institutions and coordinate study data for multi-center trials when applicableDemonstrate knowledge of the research process, Code of Federal Regulations, and International Council for Harmonisation Good Clinical Practice (ICH-GCP) guidelinesPerform accurate data collection and data entry in accordance with institutional guidelinesApply current NCI Common Toxicity Criteria and institutional reporting requirements in daily research activitiesPatient CareEvaluate patient responses to treatment and grade toxicities and adverse treatment reactionsAssess patients through personal interviews, medical record review, and communication with patients, family members, and local physiciansProvide quality patient care based on diagnosis, treatment plan, age group, developmental considerations, and identified patient needsEducate patients and families regarding treatment management, clinical trial participation, evaluation processes, and follow-up requirementsSynthesize information obtained through direct and telephone interactions to support patient care and protocol complianceAdditional DutiesPerform other duties as assigned by leadership and the department to support research and patient care objectivesEDUCATIONRequired: Graduation from an accredited school of professional nursingPreferred: Bachelor's Degree NursingWORK EXPERIENCERequired: One year Registered nurse experiencePreferred: Experience with oncology care and prior research experience is a plus.LICENSES AND CERTIFICATIONSRequired: RN - Registered Nurse - State Licensure Current State of Texas Professional Nursing license (RN) Upon Hire and a BLS - Basic Life Support Upon Hire or a CPR - Cardiac Pulmonary Resuscitation Upon HirePreferred: ACLS - Advanced Cardiac Life Support Certification as required by patient care area Upon Hire and a PALS - Pediatric Advanced Life Support Certification as required by patient care area Upon HireThe 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.