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Tennessee Oncology

Community-based cancer care with clinical research

Research Nurse

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeNashville, TN, USANo salary listed

About the Job

Requirements

  • An associate degree in nursing is required; a bachelor's degree is preferred.
  • An active registered nurse license is required.
  • Two years of nursing experience are required.
  • Knowledge of medical and research terminology is required.
  • Knowledge of the Food and Drug Administration Code of Federal Regulations and Good Clinical Practice is required.
  • Knowledge of clinical research processes is required.

Responsibilities

  • Recruit, screen, enroll, treat, and follow up with eligible clinical-trial participants according to protocol requirements.
  • Educate patients about study requirements and expectations.
  • Complete and document the informed consent process, including obtaining HIPAA authorization, and maintain informed consent throughout each study.
  • Review study design and inclusion and exclusion criteria with physicians and patients.
  • Complete and submit on-study forms within required timelines.
  • Maintain accurate source documentation of study-visit findings and outcomes.
  • Screen new and returning patients with scan results and document findings on patient-tracking logs.
  • Monitor subjects throughout studies for protocol compliance and patient safety.
  • Ensure medications are approved before treatment initiation or changes to medication regimens.
  • Dispense oral investigational products and guide participants on medication-regimen compliance.
  • Calculate and document body surface area, creatinine clearance, urine protein-to-creatinine ratio, and other protocol-required calculations or conversions.
  • Schedule follow-up appointments, scans, and related procedures according to protocol requirements.
  • Record and report adverse events according to study protocols and regulatory requirements.
  • Document when patients are removed from a protocol.
  • Obtain and document patient reconsent at the next scheduled visit when an updated informed consent form is available.
  • Provide patient education and medical information to support understanding of medication dosage, administration, and disease treatment.
  • Maintain medication inventory and reconciliation.
  • Collaborate with the clinical research team to complete study-related tasks and reporting on time.
  • Serve as a liaison among study participants, investigators, and the research team to address questions and concerns.
  • Float to other Tennessee Oncology clinics as needed.

Desired Qualifications

  • At least one year of oncology experience is preferred.
  • At least one year of experience in a research setting is preferred.
  • Research certification from ACRP or CCRP is preferred.

About the Company

Tennessee Oncology

Community-based cancer care with clinical research

Tennessee Oncology runs a large network of community-based cancer care with a strong clinical-trial program. It delivers cancer treatment at local clinics, including on-site chemotherapy, and uses molecular diagnostics to tailor therapies to each patient’s cancer. The organization supports patients with its in-house Park Pharmacy, which stocks oncology and hematology medications and handles insurance, prior authorizations, co-pays, and 24/7 pharmacist access. It differentiates itself by combining extensive community-based care with a sizable research network and a partnership with OneOncology, enabling broad access to trials and advanced care at convenient locations. The goal is to provide high-quality cancer care and access to clinical research close to patients’ homes.

Company size
501-1,000
Company stage
Debt Financing
Total funding
$98.3M
Headquarters
Nashville, TN
Founded
1976

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