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Clinical Research Rn Jobs in Tucson, AZ (NOW HIRING)

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$17

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$60

How much do clinical research rn jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for clinical research rn in Tucson, AZ is $42.57, according to ZipRecruiter salary data. Most workers in this role earn between $35.00 and $50.53 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.

What are popular job titles related to Clinical Research Rn jobs in Tucson, AZ?

For Clinical Research Rn jobs in Tucson, AZ, the most frequently searched job titles are:

What job categories do people searching Clinical Research Rn jobs in Tucson, AZ look for?

The top searched job categories for Clinical Research Rn jobs in Tucson, AZ are:

Clinical Research Rn jobs near you
Infographic showing various Clinical Research Rn job openings in Tucson, AZ as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 17% Part Time, and 9% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $88,536 per year, or $42.6 per hour.

Clinical Research Coordinator I - Nurse

Tucson, AZ

Iterative Health
See more jobs at Iterative Healthexternal

$65K - $81K/yr

Full-time

Re-posted 22 days ago

Job description

A Clinical Research Coordinator I - RN at Iterative Health is an essential member of the site research team, supporting, facilitating, and coordinating the daily execution of clinical trials across our network. This role is at the heart of every study - managing patient interactions, ensuring protocol compliance, maintaining data integrity, and keeping the operational machinery of clinical research running smoothly. 

The ideal candidate brings clinical research experience, a patient-first mindset, strong attention to detail, and the ability to thrive in a fast-paced, protocol-driven environment. This role provides a strong foundation for success while offering a clear path for professional growth within Iterative Health's expanding site network. 

Where You'll Drive Impact
  • Administratively and clinically manage industry-sponsored clinical trials, including problem-solving, communication, and protocol management.
  • Schedule all patient research visits and procedures in accordance with protocol requirements.
  • Ensure relevant study and subject-specific information is entered into the CTMS on a regular basis.
  • Complete and maintain study documentation including consent forms, source documentation, progress notes, case report forms, and investigational accountability forms.
  • Complete and maintain case report forms per FDA guidelines, reviewing them against patient medical records for completeness and accuracy.
  • Schedule and prepare for monitor visits.
  • Maintain inventory of study equipment and supplies onsite at all times.
  • Lead patient recruitment activities including chart reviews, protocol discussions with patients, and verification of informed consent documentation.
  • Conduct patient visits as outlined within each study protocol.
  • Act as the primary point of contact for study participants throughout the course of the study.
  • Dispense study medication, collect vital signs, and perform ECGs per protocol.
  • Perform blood draws; process and ship specimens per study protocol and IATA regulations.
  • As assigned: place IVs, administer IV medications and fluids, give intramuscular and subcutaneous injections, monitor patients during infusion, and discharge patients in accordance with protocol and site policies.
  • Adhere to Research SOPs, Good Clinical Practice (GCP) guidelines, and study protocols at all times.
  • Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocols.
  • Ensure all safety data is reviewed by the PI in a timely manner.
  • Cooperate with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI; report instances of noncompliance to the appropriate compliance office.
  • Assist the study team in protecting the rights and welfare of all human research participants in accordance with federal regulations.
  • Maintain ongoing communication with the CRO, sponsor, research participants, Site Manager, and PI throughout the course of each study.
  • Actively participate in communication of status and results to management.
  • Perform job related duties as requested 

What You Bring to the Team

  • Active Registered Nurse (RN) license required.
  • 1-2 years of clinical research experience strongly preferred .
  • Solid nursing background with a concentration in, or willingness to develop advanced knowledge of, GI specialty.
  • Ability to execute research tasks with guidance from experienced staff, PIs, and management.
  • Strong written and verbal communication skills.
  • Ability to read, interpret, and apply clinic policies and research protocols.
  • Proficiency in standard office software and CTMS platforms.
  • Highly organized with the ability to manage multiple priorities and meet deadlines.
  • Ability to work independently and collaboratively in a fast-paced environment.
Preferred Qualifications
  • Prior GI or hepatology clinical research experience.
  • Familiarity with GCP guidelines and FDA regulations governing clinical research.
  • Experience with CTMS, EDC, or eTMF platforms.
  • ACRP or SOCRA certification (CCRC or CCRP), or active pursuit of certification.

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