Clinical Research Nurse II, Cancer Center (Full-time)

The University of Arizona Cancer Center (UACC) is a National Cancer Institute-designated Comprehensive Cancer Center committed to preventing and curing cancer through exceptional patient care, groundbreaking research, and comprehensive education.

The Clinical Trials Office is searching for a Clinical Research Nurse. This position would be responsible for coordinating the clinical care of research patients and ensuring research patient safety. Oncology clinical trial drugs have varying levels of toxicity, and Research Nurses are responsible for monitoring and assessing patient responses and adverse events. Research Nurses educate patients on drug safety and keep clinical research coordinators, physicians and clinical staff appraised on patient status. Each Research Nurse works with an average of 8-20 active patients on 8-15 active studies, depending on the complexity and phase of the clinical trial. The Research Nurse is involved in the clinical research process from the time of the site evaluation visit, site initiation visit and start up, all the way to patients completing treatment on a trial.

Outstanding UA benefits include health, dental, and vision insurance plans; life insurance and disability programs; paid vacation, sick leave, and holidays; UA/ASU/NAU tuition reduction for the employee and qualified family members; retirement plans; access to UA recreation and cultural activities; and more!

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Primary Clinical Research Nurse for Oncology Clinical Trials:

• Plan, coordinate, and evaluate nursing care of oncology clinical trial participants on IRB approved clinical trial protocols.
• Perform procedures that require a nursing license, within the guidelines of institutional policy.
• Work with a clinical research team to create plans to confirm proper execution of clinical trial procedures
• Participate in protocol development by reviewing potential protocols and evaluating their effect on standard nursing procedures
• Prepare for and attend Site Evaluation Visits and Site Initiation Visits.

Participate in Training:

• Participate in training and staff meetings
• Develop and provide educational material and training to patients, family members, and clinical staff to ensure patient safety and adherence to protocols

Provide Direct Patient Care:

• Coordinate and/or perform physical assessments, administer medications, and order and coordinate additional lab tests and other protocol required procedures
• Perform peripheral blood sampling as well as blood sampling from ports and IV catheters following our medical partner's guidelines, and as required by clinical trial protocols. Work with the Specimen Management team to ensure samples are processed appropriately
• Ensure patient safety by assessing and documenting adverse events and documenting concomitant medications
• Provide patient education regarding study drug dosing, adverse events, and supportive care
• Support PI/treating physicians with protocol adherence regarding study medication dosing calculations, toxicity management, supportive care, and communication with study sponsors about clinical issues
• Utilize guidance materials for clinical partner nursing staff to properly and safely administer clinical trial treatments

Maintain Proper Communication and Collect Appropriate Data:

• Adhere to ALCOA guidelines while maintaining diligent nursing documentation
• Communicate regularly with patients to assess toxicities and provide guidance and document assessments appropriately
• Communicate regularly with physicians and clinical partner staff to coordinate supportive care for patients as needed
• Communicate with sponsors and other study personnel as necessary

Other Duties as Assigned

Knowledge, Skills, and Abilities:

• Demonstrated strong interpersonal, communication, and problem solving skills.
• Excellent organizational skills.
• Comfortable with navigating electronic databases.
• Attention to detail.

• Bachelor's degree or equivalent advanced learning attained through professional level experience required.
• Minimum of 3 years of relevant work experience, or equivalent combination of education and work experience.

• Previous work in oncology and/or research nursing.
• Previous work with different Electronic Medical Record Systems.
• Demonstrated detailed documentation skills.