Research RN in Chandler, Arizona at IRONWOOD PHYSICIANS,P.C.

Join one of the Southwest's premier oncology research programs. Our rapidly expanding Research Department delivers innovative cancer clinical trials across eight Phoenix-area locations, providing patients with access to some of the most promising new therapies available. Recognized as a preferred site by leading industry sponsors, we have contributed to numerous landmark studies that have led to FDA-approved treatments. Our renowned physician investigators are deeply engaged in research and are widely recognized for their expertise and leadership. Together, we are shaping the future of cancer care while bringing hope and cutting-edge treatment options to our community. Our Research Department is an integral part of the care offered at our cancer centers.

We are seeking a dynamic, autonomous, and knowledgeable Research Nurse. This position offers excellent opportunities for rapid professional growth in a collaborative and diverse workplace. The Research Nurse manages and coordinates all aspects of conducting clinical trials, both clinically and administrative/regulatory. Required to have in-depth knowledge of protocol requirements and ensures that studies are properly conducted in conformance with the protocol guidelines, departmental standards and good clinical practices as set forth by federal regulations and international guidelines. The position is full time, Monday through Friday. No call or weekends.

Essential Duties & Responsibilities:

Reviews studies for clinical and operational feasibility, along with the Investigator and Director of Research. Screens, consents, enrolls and follows study subjects and oversees the same by non-RN clinical research coordinators, ensuring protocol compliance and close monitoring while subjects are on study. Responsible for all data and source documentation, adverse experience reporting, and will assist Regulatory Specialist in the maintenance of complete regulatory files. Responsible for following departmental policies and assuring proper billing for research subjects. Assists as needed in preparing study for submission to IRB and ensures all regulatory documents are completed. Ensures that randomization procedures and blinding procedures, as applicable, are followed as per protocol guidelines. Ensures eligible patients are enrolled and that consent process is appropriate and in compliance with all standards. Responsible for quality data entry into sponsor’s database (electronic data capture systems or paper CRFs) and query resolution. Prepares, mixes and administers investigational product, as applicable. Ensures proper study drug administration, compliance and accountability, including receipt, storage and dispensing.

Excellent clinical and functional skills. Organized and detail oriented. Strong leadership skills. Strong communication and team building skills a must. Computer skills required (Microsoft office). Willing to travel between offices.

Clinical Oncology and/or prior research experience required. Graduation from an accredited School of Nursing. Bachelor’s degree preferred. Current IATA, Human subjects protection training or GCP training highly desirable. Arizona RN license in good standing. Specialty certification such as CCRC preferred.