Research RN-Chandler

Ironwood Cancer and Research Centers•Chandler, AZ

13d•Onsite

About The Position

Ironwood Cancer & Research Centers is seeking a dynamic, autonomous, and knowledgeable Research Nurse to manage and coordinate all clinical and administrative/regulatory aspects of clinical trials. The Research Department conducts cancer clinical trials across eight Phoenix-area locations and works with physician investigators and industry sponsors to provide patients access to promising therapies. The Research Nurse must understand protocol requirements and ensure studies are conducted in accordance with protocol guidelines, departmental standards, good clinical practices, federal regulations, and international guidelines. This is a full-time position, Monday through Friday, with no call or weekend work. Travel between offices is required.

Requirements

Clinical oncology and/or prior research experience required.
Graduation from an accredited School of Nursing.
Current Arizona RN license in good standing.
Excellent clinical and functional skills.
Strong organizational and detail-oriented skills.
Strong leadership skills.
Strong communication and team-building skills.
Computer skills, including Microsoft Office.
Willingness to travel between offices.

Nice To Haves

Bachelor’s degree preferred.
Current IATA, human subjects protection, or GCP training highly desirable.
Specialty certification such as CCRC preferred.

Responsibilities

Review studies for clinical and operational feasibility with the Investigator and Director of Research.
Screen, consent, enroll, and follow study subjects; oversee non-RN clinical research coordinators performing these activities and ensure protocol compliance and close monitoring of subjects.
Maintain data and source documentation, report adverse experiences, and assist the Regulatory Specialist with complete regulatory files.
Follow departmental policies and ensure proper billing for research subjects.
Assist with preparing studies for IRB submission and ensure regulatory documents are completed.
Ensure randomization and, when applicable, blinding procedures are followed according to protocol guidelines.
Ensure eligible patients are enrolled and that the consent process complies with applicable standards.
Enter high-quality data into sponsor databases, including electronic data capture systems or paper CRFs, and resolve queries.
Prepare, mix, and administer investigational products when applicable.
Ensure proper study drug administration, compliance, and accountability, including receipt, storage, and dispensing.