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Clinical Research Nurse

2 months ago


Houston, Texas, United States MD Anderson Cancer Center Full time

MISSION STATEMENT

The University of Texas M. D. Anderson Cancer Center is dedicated to the eradication of cancer through exceptional programs that merge patient care, research, and prevention, alongside educational initiatives for students, trainees, professionals, and the public.

SUMMARY

The primary objective of the Clinical Research Nurse role is to support the clinical and operational oversight of research protocols.

Ideal Candidate Profile

The preferred candidate for the Clinical Research Nurse position will possess a minimum of two years of experience as a Registered Nurse, with a background in Med/Surg, Oncology, or Urology being advantageous.

CORE VALUES

Caring Behaviors

Courtesy: Maintain respect and politeness towards colleagues and patients at all times.

Friendliness/Teamwork: Foster and celebrate teamwork and inclusivity; remain attuned to the concerns of patients and coworkers.

Integrity Behaviors

Reliability: Engage in frequent, honest, and transparent communication.

Accountability: Hold oneself and others responsible for upholding our values.

Safety: Identify safety issues and address them promptly; exemplify safe practices.

Discovery Behaviors

Responsiveness: Cultivate an atmosphere of trust through actions; promote learning, creativity, and innovation.

Personal Leadership/Self-Initiative: Assist others in problem identification and resolution; pursue personal development and encourage the same in others.

KEY FUNCTIONS

  • Conduct assigned research protocol operations in compliance with FDA and ICH Good Clinical Practice guidelines. Utilize clinical and research expertise for effective protocol management and assess patient eligibility for studies in collaboration with physicians.
  • Successfully recruit patients for clinical and minimal risk trials.
  • Exhibit a thorough understanding of the research process, federal regulations, and ICH Good Clinical Practice guidelines.
  • Coordinate, assess, and monitor patient involvement in clinical trials, assisting in data collection and evaluation. Develop patient care methodologies for protocols, including eligibility criteria.
  • Independently execute protocol-specific clinical tasks such as patient assessment, screening, scheduling, ordering tests, specimen collection, and monitoring responses; may administer medications as needed, adhering to nursing protocols.
  • Implement educational strategies to address patient and family learning needs, providing information regarding treatment management and follow-up in clinical trials through direct communication or written materials.
  • Oversee the effective operation of designated protocols, ensuring appropriate charges and reimbursements for patient-related protocol expenses.
  • Demonstrate proficiency in data collection and entry, adhering to institutional guidelines. Collaborate with primary investigators in data collection and maintain accurate patient records in compliance with relevant standards.
  • Evaluate treatment responses, toxicities, and adverse reactions, reporting findings to the principal investigator and relevant oversight bodies.
  • Participate in start-up meetings for new protocols, preparing logistics and coordinating activities with primary investigators.
  • Apply nursing principles and national standards in delivering care to patients enrolled in research protocols, documenting care and outcomes according to institutional and protocol standards.
  • Ensure compliance with all standards, policies, and quality measures for research staff involved in protocols.
  • Notify relevant personnel of upcoming audits and prepare necessary documentation for audits and monitoring visits.
  • Communicate effectively with the research team and orient faculty/support staff on study protocols.
  • Possess the ability to travel between various care areas and maintain an organized work environment.
  • Engage in continuing education and professional development opportunities, maintaining required licenses and certifications.
  • Attend monthly research team meetings and complete all mandatory training.
  • Perform additional duties as assigned.

EDUCATION

Required: Graduation from an accredited nursing program.

Preferred: Bachelor’s Degree in Nursing.

EXPERIENCE

Required: Two years of experience as a Registered Nurse.

Preferred: Two years of experience in Clinical Research.

It is the policy of The University of Texas MD Anderson Cancer Center to provide equal employment opportunities 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.