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IRONWOOD PHYSICIANS,P.C.

Research RN

Chandler, AZ · On-site

Research RN Full-time Regular Chandler, AZ, US 11 days ago Requisition ID: 8210 Ironwood Cancer ... Our rapidly expanding Research Department delivers innovative cancer clinical trials across eight ...

Hux Cancer Center

RN - Clinical Research

Terre Haute, IN · On-site

$2.6K/wk

Details Client Name Hux Cancer Center Job Type Travel Offering Nursing Profession RN Specialty Clinical Research Job ID 19079371 Job Title RN - Clinical Research Weekly Pay $2656.0 Shift Details ...

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How much do clinical research rn jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for clinical research rn in the United States is $44.13, according to ZipRecruiter salary data. Most workers in this role earn between $36.30 and $52.40 per hour, depending on experience, location, and employer.

What is a clinical research RN?

Clinical Research Registered Nurses (Clinical Research RNs) are licensed nurses who specialize in conducting and coordinating clinical trials and research studies involving human participants. They collaborate with physicians, researchers, and study coordinators to ensure that research protocols are followed, participants are cared for safely, and all regulatory and ethical guidelines are met. Their duties include administering study medications, collecting data, monitoring patient responses, and educating participants about the study. Clinical Research RNs play a vital role in advancing medical knowledge and improving patient care through research.

How does a clinical research RN typically collaborate with other members of the research team?

A Clinical Research RN works closely with principal investigators, study coordinators, physicians, and data managers to ensure research protocols are followed accurately and patient safety is maintained. They are responsible for communicating patient progress, reporting adverse events, and coordinating care between departments. Regular team meetings and detailed documentation are essential to keep everyone informed and maintain compliance with regulatory standards. This collaborative environment helps ensure research studies run smoothly and efficiently.

What are the key skills and qualifications needed to thrive as a clinical research RN, and why are they important?

To thrive as a Clinical Research RN, you need a solid background in nursing, clinical trial protocols, and regulatory compliance, typically requiring an RN license and experience in research settings. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification is often expected. Excellent organizational, communication, and critical thinking skills help you coordinate studies, interact with participants, and collaborate with multidisciplinary teams. These competencies ensure the integrity of research data, patient safety, and successful execution of clinical trials.

What is the difference between Clinical Research Rn vs Clinical Research Coordinator?

AspectClinical Research RnClinical Research Coordinator
CredentialsRN license, possibly specialized certificationsTypically bachelor's degree, certifications like CCRP beneficial
Work EnvironmentHospitals, clinics, research institutionsResearch sites, hospitals, clinics
Job FocusPatient care, protocol adherence, data collectionStudy coordination, participant recruitment, data management

While both roles are involved in clinical research, the Clinical Research Rn primarily provides patient care and ensures protocol compliance from a nursing perspective. The Clinical Research Coordinator manages study logistics, participant recruitment, and data collection. Both roles require strong organizational skills, but the RN's focus is more on patient interaction, whereas the Coordinator handles study operations.

How to get into clinical research as a registered nurse?

To become a clinical research RN, obtain a valid nursing license and gain experience in patient care. Additional certifications such as Certified Clinical Research Professional (CCRP) or Good Clinical Practice (GCP) training can improve job prospects, and familiarity with research protocols and data management is beneficial.

What do clinical research RNs do in clinical research?

Clinical research RNs coordinate and monitor clinical trials by recruiting participants, collecting data, administering treatments, and ensuring compliance with study protocols and regulations. They often work closely with investigators, maintain accurate documentation, and may require certification such as CCRP. Their role is essential for the safe and effective conduct of research studies.
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Clinical Research Rn jobs near you
Infographic showing various Clinical Research Rn job openings in the United States as of September 2026, with employment types broken down into 3% As Needed, 73% Full Time, 16% Part Time, and 8% Contract. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $91,797 per year, or $44.1 per hour.

Research RN

Chandler, AZ • On-site

IRONWOOD PHYSICIANS,P.C.
See more jobs at IRONWOOD PHYSICIANS,P.C.external

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Medical, Dental, Vision, Life, Retirement

Re-posted 24 days ago

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

Full-time Regular Chandler, AZ, US

11 days ago Requisition ID: 8210

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

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