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Clinical Research Rn Jobs in Tennessee (NOW HIRING)

Actalent

Oncology Clinical Research Nurse

Nashville, TN · On-site

$75K - $102K/yr

  • Retirement

  • PTO

Registered Nurse (VERY competitive benefits) Responsible for hands-on role in clinical trial execution as a Registered Nurse, combining direct patient care expertise with research protocol compliance

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How much do clinical research rn jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for clinical research rn in Tennessee is $40.06, according to ZipRecruiter salary data. Most workers in this role earn between $32.93 and $47.55 per hour, depending on experience, location, and employer.

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 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 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 CCRN or CCRA. Their role is essential for ensuring the safety of participants and the integrity of the research data.

What are popular job titles related to Clinical Research Rn jobs in Tennessee?

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

What job categories do people searching Clinical Research Rn jobs in Tennessee look for?

The top searched job categories for Clinical Research Rn jobs in Tennessee are:

What cities in Tennessee are hiring for Clinical Research Rn jobs?

Cities in Tennessee with the most Clinical Research Rn job openings:

Clinical Research Rn jobs near you
Infographic showing various Clinical Research Rn job openings in Tennessee as of August 2026, with employment types broken down into 89% Full Time, 9% Part Time, and 2% Contract. Highlights an 100% In-person job distribution, with an average salary of $83,317 per year, or $40.1 per hour.

Coordinator-Research Nurse I RN

Baptist Memorial Healthcare Corporation

Memphis, TN • On-site

$61K - $77K/yr

Other

Re-posted 25 days ago

Job description


Job Summary
The Research Coordinator, RN- I is responsible for coordinating the conduct of research protocols, assuring that the integrity and quality of the research is maintained and that the research is conducted in accordance with Good Clinical Practice Guidelines, federal, and sponsor regulations and guidelines, BMHCC and BCRI policies and procedures. This includes the coordination of clinical research activities, patient clinical care and management, recruitment, screening, scheduling, enrollment, submission of data, randomization and patient follow-up. This position may act as a liaison between the hospital, the IRB, study sponsors, and all investigators. This position will collaborate with research coordinators, data managers and regulatory specialists. Travel may be required.
Responsibilities
  • Facilitates compliance with the requirements of the research protocol and good clinical practice while remaining cognizant of the needs of diverse patient populations.
  • Communicates with research team to facilitate the effective conduct of clinical trials.
  • Demonstrates leadership in ensuring patient comprehension and safety during initial and ongoing clinical trial informed consent discussions.
  • Manages the activities of patients participating in clinical trials, ensuring compliance with protocol procedures, assessments, and reporting requirements.
  • Ensures collection of source data and completion of documentation that validate the integrity of the conduct of the clinical trial.
  • Enhances recruitment while being mindful of the needs of diverse patient populations.
  • Enhances adherence to ethical practices during the conduct of clinical trials in order to protect the rights and well-being of patients and the collection of quality data.
  • Identifies financial variables that affect research and supports good financial stewardship in clinical trials.
  • Identifies his or her ongoing professional development needs and seeks resources and opportunities to meet those needs, such as memberships in nursing, oncology, or research organizations.
  • Other responsibilities as assigned.
Specifications
Experience
Minimum Required
  • 2 years of Research or Clinical experience
Preferred/Desired
  • 2 years of Oncology or Clinical Research Experience
Education
Minimum Required
  • Currently licensed nurse or equivalent combination of education and experience
Preferred/Desired
  • Preferred/Desired bachelors degree in Nursing.
Special Skills
Minimum Required
Preferred/Desired
  • Computer skills to include MS Word, Excellent organizational skills. Detail oriented. Experience with EMR and Clinical Trial Management System
Licensure
Minimum Required
  • BLS certification within 14 days; RN License required by state.
Preferred/Desired
  • Certifications - SOCRA (Society of Clinical Research Associates), ACRP (Association of Clinical Research Professionals), Collaborative Institutional Training Initiative (CITI), HAZMAT, CCRP or CCRC

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