Research RN-Surprise

Ironwood Cancer and Research Centers•Surprise, AZ

About The Position

Ironwood Cancer & Research Centers is seeking a dynamic, autonomous, and knowledgeable Research Nurse to join its expanding oncology research program. The Research Department conducts cancer clinical trials across eight Phoenix-area locations, working with physician investigators and industry sponsors to provide patients with access to promising therapies. The Research Nurse manages and coordinates the clinical, administrative, and regulatory aspects of clinical trials, applying detailed knowledge of protocol requirements and ensuring studies are conducted according to protocol, departmental standards, good clinical practices, and applicable federal regulations and international guidelines. The position is full-time, Monday through Friday, with no call or weekend work. The role offers opportunities for professional growth in a collaborative and diverse workplace and requires travel between offices.

Requirements

Clinical oncology experience and/or prior research experience.
Graduation from an accredited School of Nursing.
Current Arizona RN license in good standing.
Excellent clinical and functional skills.
Organized and detail-oriented.
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.
Current IATA, human subjects protection training, or GCP training.
Specialty certification such as CCRC.

Responsibilities

Review studies for clinical and operational feasibility with the Investigator and Director of Research.
Screen, consent, enroll, and follow study subjects, and oversee non-RN clinical research coordinators in these activities, ensuring 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 blinding procedures are followed according to protocol, as applicable.
Ensure eligible patients are enrolled and that the consent process complies with applicable standards.
Enter quality data into sponsor databases, including electronic data capture systems or paper CRFs, and resolve queries.
Prepare, mix, and administer investigational products, as applicable.
Ensure proper study drug administration, compliance, accountability, receipt, storage, and dispensing.