Oncology Clinical Research Nurse — Impactful Trials

Sarah Cannon Research Institute

Nashville (TN)

Presencial

USD 70 000 - 90 000

Tempo integral

Há 4 dias
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Resumo da oferta

Sarah Cannon Research Institute (SCRI) in the Nashville area is seeking a Clinic Research Nurse to ensure protocol compliance and monitor study subjects throughout treatment.

You will screen and enroll patients, document visits, calculate essential measurements per protocol, schedule follow-ups, and coordinate with SCRI and clinic staff to keep trials on track and patients safe. SCRI emphasizes rigorous research standards and patient-centered care.

Qualificações

  • RN license and oncology exposure preferred.
  • Knowledge of FDA CFRs and GCP required or preferred.
  • Experience with clinical research processes and documentation.
  • Familiarity with screening, enrollment and protocol adherence.
  • ACRP or CCRP certification preferred.

Responsabilidades

  • Follow study subjects to ensure protocol compliance and safety.
  • Screen, treat, and monitor patients per protocol as the primary tool.
  • Complete patient documentation at each clinic visit and during screening.
  • Ensure medications are approved by the registrar before treatment changes.
  • Calculate and document BSA, creatinine clearance, and other conversions as required.
  • Schedule follow-up appointments, scans, and procedures per protocol requirements.
  • Inform SCRI and clinic staff when a patient comes off study.

Conhecimentos

RN License
Medical terminology
Regulatory knowledge (FDA CFR, GCP)
Clinical research processes
Oncology experience
Research setting experience
ACRP/CCRP certification

Formação académica

Associate degree
Bachelor's degree preferred

Descrição da oferta de emprego

Sarah Cannon Research Institute (SCRI) in the Nashville area is seeking a Clinic Research Nurse to ensure protocol compliance and monitor study subjects throughout treatment.

You will screen and enroll patients, document visits, calculate essential measurements per protocol, schedule follow-ups, and coordinate with SCRI and clinic staff to keep trials on track and patients safe. SCRI emphasizes rigorous research standards and patient-centered care.

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