Research RN-Chandler

Ironwood Women's Centers; Chandler, Northern (AZ, KY); Hybrid; USD 85,000 - 110,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

Life insurance

401K

Job summary

Ironwood Cancer & Research Centers in Chandler, AZ seeks a dynamic Research Nurse to manage and coordinate all aspects of clinical trials within a premier cancer care network. The role requires strong oncology knowledge, nursing credentials, and careful regulatory oversight, with travel between offices as needed.

The position is full-time, Monday through Friday, with opportunities for rapid professional growth in a collaborative, diverse setting and a comprehensive benefits package including

Qualifications

• Clinical Oncology and/or prior research experience required.
• Bachelor’s degree in Nursing preferred.
• Current IATA, Human subjects protection training or GCP training highly desirable.
• Specialty certification such as CCRC preferred.

Responsibilities

• Reviews clinical studies for feasibility and protocol compliance.
• Screens, consents, enrolls and follows study subjects; supervises coordinators.
• Maintains regulatory files and ensures proper billing for research subjects.
• Prepares study materials for IRB submission and ensures regulatory documents are complete.
• Ensures correct randomization and blinding procedures per protocol.

Education

Bachelor's degree in Nursing

IATA/Good Clinical Practice (GCP) training

Specialty certification such as CCRC

Tools

Microsoft Office

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Research RN-Chandler

Full-time Regular Chandler, AZ, US

Ironwood Cancer & Research Centers has beautiful state-of-the-art integrated Cancer and Women's Centers, with locations strategically located throughout the Valley. Each one provides a superior cancer care environment with a full spectrum of cancer related services for patients. Our multi-disciplinary team approach includes surgical oncology, medical oncology, radiation oncology, women's centers, diagnostic imaging services, social service support, nutritionist, integrative services, and genetic counseling.
Mission Statement: To serve the community by providing quality, comprehensive cancer care which respects the values and needs of each individual.
Overview:

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.

Knowledge and Skills:

• 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.

Qualifications:

• 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.
• Specialty certification such as CCRC preferred.

We offer a competitive salary and a comprehensive benefit package including health/dental/vision, life insurance, and 401K, in a caring work environment. We are an E.O.E.

Please visit our website at www.ironwoodcrc.com. "Outsmarting Cancer One Patient at a Time"