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Clinical Research Rn Jobs in Tennessee (NOW HIRING)

Covenant Health

Clin Research Nurse Coord

Knoxville, TN · On-site

$65K - $82K/yr

Overview Registered Nurse Coordinator, Oncology Clinical Research Full Time, 80 Hours Per Pay Period, Day Shift Thompson Cancer Survival Center Overview: Thompson Cancer Survival Center is our region ...

Covenant Health

Clin Research Nurse Coord

Knoxville, TN

$65K - $82K/yr

Registered Nurse Coordinator, Oncology Clinical Research Full Time, 80 Hours Per Pay Period, Day Shift Thompson Cancer Survival Center Overview: Thompson Cancer Survival Center is our region ...

Medix

Clinical Research Coordinator

Nashville, TN · On-site

$25.93 - $32.41/hr

Bachelor's degree in a health-related field such as nursing, biology, or public health preferred. * Prior experience in clinical research or oncology preferred. * Knowledge of clinical trial ...

ICON

Senior Clinical Research Associate

Knoxville, TN · On-site +1

A graduate with a Bachelor's degree in Life Sciences or equivalent, or a qualified RN * Eligible to work in United States without visa sponsorship * A clinical research professional with 3+ years of ...

Tennessee Oncology

Research Nurse

Nashville, TN · On-site

Knowledge of the clinical research processes Education & Experience: * An associate degree in nursing, preferably a bachelor's degree * RN License * 2 years of nursing experience required. * At least ...

Tennessee Oncology

Research Nurse

Clarksville, TN · On-site

Knowledge of the clinical research processes EDUCATION & EXPERIENCE: * An associate degree in nursing, preferably a bachelor's degree * RN License * 2 years of nursing experience required. * At least ...

Tennessee Oncology

Research Nurse

Nashville, TN · On-site

Knowledge of the clinical research processes EDUCATION & EXPERIENCE: * An associate degree in nursing, preferably a bachelor's degree * RN License * 2 years of nursing experience required. * At least ...

Tennessee Oncology

Research Nurse

Nashville, TN · On-site

Knowledge of the clinical research processes EDUCATION & EXPERIENCE: * An associate degree in nursing, preferably a bachelor's degree * RN License * 2 years of nursing experience required. * At least ...

Tennessee Oncology

Research Nurse

Nashville, TN · On-site

Knowledge of the clinical research processes EDUCATION & EXPERIENCE: * An associate degree in nursing, preferably a bachelor's degree * RN License * 2 years of nursing experience required. * At least ...

Tennessee Oncology

Research Nurse

Clarksville, TN

Knowledge of the clinical research processes EDUCATION & EXPERIENCE: * An associate degree in nursing, preferably a bachelor's degree * RN License * 2 years of nursing experience required. * At least ...

Tennessee Oncology

Research Nurse

Clarksville, TN · On-site

Knowledge of the clinical research processes EDUCATION & EXPERIENCE: * An associate degree in nursing, preferably a bachelor's degree * RN License * 2 years of nursing experience required. * At least ...

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Clinical Research Rn information

See Tennessee salary details

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$57

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.

Clin Research Nurse Coord

Covenant Health

Knoxville, TN • On-site

$65K - $82K/yr

Full-time

Re-posted 4 days ago

Job description

Overview
Registered Nurse Coordinator, Oncology Clinical Research
Full Time, 80 Hours Per Pay Period, Day Shift
Thompson Cancer Survival Center Overview:
Thompson Cancer Survival Center is our region's largest cancer-fighting network, with more imaging centers, more board-certified physicians and surgeons, and more cancer and radiation centers closer to where you call home. And, we are a proud member of Covenant Health, our region's top-performing healthcare network with 10 hospitals, outpatient and specialty services, and Covenant Medical Group, our area's fastest-growing physician practice division.
Thompson Cancer Survival Center (TCSC) was founded to bring world-class cancer care to East Tennessee. At Thompson, leading cancer specialists use the most advanced technologies to achieve breakthrough successes in treating many types of cancer. Our doctors have the support of a complete team: Dieticians, genetics counselors, physicists, pharmacists, therapists, technologists, oncology nurses, social workers and others are all there to treat - and beat - the disease.
Position Summary:
The Clinical Research Nurse Coordinator promotes good clinical practices in the conduct of oncology clinical trials by possessing in-depth knowledge of federal regulations and guiding documents for the conduct of clinical trials and human participant protection. In addition, the Clinical Research Nurse Coordinator assures compliance with protocol and regulatory requirements, manages patient protocol activities, assures patient safety, collects records and maintains data and source documentation. The Clinical Research Nurse Coordinator performs all the duties and responsibilities associated with high-level, professional nursing practice including autonomous decision making based on predetermined protocol guidelines, nursing assessment and oncology knowledge. Reports to the Clinical Trials Manager.
Responsibilities
Trial Planning and Strategy
  • Participates in protocol planning by applying knowledge of patient population and anticipated recruitment, considering the ability to maintain the rights, safety, and well-being of the patient and serving as the liaison between the investigator and the sponsor to clarify expectations, goals, procedures, questions, and concerns.
  • Plans and implements pre-study activities by developing timelines for conducting the clinical trial protocol, attending and participating in investigator meetings at the manager's discretion and scheduling and coordinating pre-study site visits, initiation visits, monitoring visits, and close-out visits.

Trial Recruitment and Management
  • Manages Subject Recruitment and Enrollment by monitoring enrollment goals and modifying the recruitment plan as necessary, maintaining patient screening/enrollment logs, reviewing information about the protocol including inclusion/exclusion criteria with investigator. Assuring that all screening, eligibility, and enrollment procedures are performed according to protocol requirements by reviewing source documents in the EMR. Attend multidisciplinary conferences/meetings to provide study-related information as needed to the physicians discussed during the conference/meeting.
  • Coordinates patient enrollment in clinical trials by following randomization procedures as per protocol, scheduling patient office visits, required screening assessments, ensuring appropriate specimen collection, batching and shipping per protocol and assessing participant compliance with the test article and follow-up visits.
  • Manages clinical trial patient by scheduling all protocol-required tests, physician and nurse assessment visits, monitoring patient's response to protocol treatment, accompanying the physician for all protocol-required visits at all offices, reporting all serious adverse effects to the appropriate agency and Covenant Health IRB according to protocol guidelines, manages/resolves complex patient/physician/clinical trial issues without supervision.

Regulatory Compliance and Safety
  • Maintains federal guidelines for Informed Consent process by communicating information about the protocol, informed consent form and follow-up procedures with potential study patients, conducting interviews to assess the patient's ability and willingness to follow and complete study procedures and visits, obtaining informed consent from the patient prior to any study-related procedures and documenting appropriately.
  • Ensures patient safety with ongoing patient education about cardiovascular treatments and disease process. Perform skilled nursing assessments and promptly report all findings to the investigator and study sponsor. Recognize laboratory values and assessments outside of normal limits.
  • Documents and maintains all study-related procedures, processes, and events by obtaining and reviewing original source documents, i.e., office notes, imaging reports, lab reports, procedure notes, etc.), abstracting data to study forms and flowsheets, recording accurate and timely data entry into electronic or hard-copy case report forms, documenting protocol deviations and exemptions, planning and designing new forms/source document tools to utilize in protocol implementation. Resolve data queries and amend case report forms as appropriate.

Resource Management
  • Maintain investigational agents and/or devices provided by study sponsor by accurately accounting for products received onsite. This includes all supplies provided by the study sponsor. Oversee the storage and integration of clinical trial product according to Covenant Health policy.

Communication and Report
  • Protect participant confidentiality by adhering to HIPAA regulations, protecting patient privacy at all times, securing safe storage of study-related documents, assuring appropriate disposal of PHI, securely storing all archived files.
  • Communicates effectively with patients, research team, IRB, study sponsor, and Clinical Trials Manager by providing protocol education to ancillary staff. Establishing a contact mechanism for participants regarding follow-up visits, new study information and instructing participants to report study-related events to the research team immediately. Effective communication with investigator and sponsor representative to ensure protocol compliance. Punctually submitting reports, making suggestions or raising concerns to the Clinical Trials Manager.

Quality Assurance
  • Participants in monitoring visits and audits by collecting source documents for sponsor review, meeting with monitors during routine visits to discuss case report form completion, query resolution, and other protocol-related issues. Prepare and participate in all audit tasks and meetings as needed.
  • Assists with reviewing and developing standard operating procedures for study-related tasks as needed. Participant in orienting and training new staff involved in study visits. Supervise clinical research associates as needed.
  • Implement Quality Controls and Assurance Measures by monitoring compliance with study procedures and GCP standards, conducting quality assurance audits as requested, working with internal and external quality assurance teams.
  • Local travel required. Will be traveling between Covenant Health Facilities as needed to meet with physicians and patients.
  • Maintains professional and technical knowledge by attending conferences at the discretion of the Clinical Trials Manager; presenting professional education to colleagues, performing self-directed study, reviewing professional publications and participating in professional societies. Completes all IT training to access various EDC systems and EMR. Be proficient with basic office software such as Microsoft Office.
  • Follows policies, procedures, and safety standards. Completes required education assignments annually. Works toward achieving goals and objectives, and participates in quality improvement initiatives as requested.
  • Performs other duties as assigned.

Qualifications
Minimum Education:
None specified; however must be sufficient to meet the standards for achievement of the below indicated license and/or certification as required by the issuing authority.
Minimum Experience:
Two (2) years of experience in cardiology nursing/relevant nursing care or two (2) years' experience in clinical trials. Excellent written and oral communication skills, project management skills. Good Interpersonal and leadership skills. Excellent computer skills.
Licensure Requirement:
Must have and maintain Tennessee RN licensure. Employee must have a valid Tennessee driver's license Class D and state mandated minimum insurance coverage. Driving record must meet Covenant Health minimum standards at the date of hire and throughout employment tenure.#cb

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