Oncology Clinical Trials Nurse (Research RN)

Sarah Cannon Research Institute

Nashville (TN)

On-site

USD 65,000 - 90,000

Full time

14 days+

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Benefits offered by this job

Total Rewards package
Competitive compensation

Job summary

Sarah Cannon Research Institute (SCRI) seeks a Clinic Research Nurse to monitor study subjects and ensure protocol compliance across oncology trials. The role emphasizes precise documentation, patient safety, and coordination with registrars for treatment approvals.

Qualified candidates will hold an RN license, have knowledge of medical terminology and CFR/GCP, and bring experience in clinical research. Oncology experience and CCRP/ACRP certification are preferred.

Qualifications

  • RN License and knowledge of medical terminology are required.
  • Familiarity with FDA Code of Federal Regulations (CFR) and Good Clinical Practice (GCP) is expected.
  • Experience in clinical research and oncology settings is preferred.
  • Healthcare research knowledge and processes should be demonstrated.
  • CCRP/ACRP certification is a plus.

Responsibilities

  • Ensure protocol compliance and monitor subjects while on study.
  • Screen, treat, and follow patients using the protocol.
  • Complete patient documentation at each clinic visit.
  • Coordinate medication approvals with the registrar for treatments and changes.
  • Accurately calculate and document clinical measurements per protocol.
  • Schedule follow-up visits, scans, and procedures as required.
  • Inform SCRI and clinic staff when a patient comes off study.

Skills

RN License
Medical & Research Terminology
FDA CFR & GCP
Clinical Research Processes
Oncology Experience
Research Setting Experience
Research Certification (ACRP/CCRP)

Education

Associate degree; preferably a bachelor’s degree

Job description

Sarah Cannon Research Institute (SCRI) seeks a Clinic Research Nurse to monitor study subjects and ensure protocol compliance across oncology trials. The role emphasizes precise documentation, patient safety, and coordination with registrars for treatment approvals.

Qualified candidates will hold an RN license, have knowledge of medical terminology and CFR/GCP, and bring experience in clinical research. Oncology experience and CCRP/ACRP certification are preferred.

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