Clinical Research Nurse

7 days ago

Nashville, Tennessee, United States Tennessee Oncology Full time
Job Description:

Job Summary:

Tennessee Oncology is seeking a highly skilled and motivated Clinical Research Nurse to join our team. As a Research Nurse, you will play a critical role in the success of our clinical trials by ensuring the protection of study patients and adhering to protocol requirements.

Key Responsibilities:

  • Enroll patients onto clinical trials through recruitment, screening, enrollment, treatment, and follow-up of eligible participants according to protocol requirements.
  • Obtain and maintain informed consents of each patient for the duration of a study.
  • Review the study design and inclusion/exclusion criteria with physician and patient.
  • Ensure the protection of study patients by verifying informed consent procedures and adhering to protocol requirements.
  • Complete and document screening/eligibility accurately.
  • Complete and document the informed consent process accurately and have all parties sign/date as required, including HIPAA Authorization.
  • Accurately complete and submit on-study forms within required timelines.
  • Document all specific tools required by the protocol (i.e., oral medication forms, pill count diaries, quality of life questionnaires, neuro exams, vital signs sheets, times of PK draws, etc.).
  • Screen every new patient or patient returning to office with scan results and document appropriately on the patient tracking logs.
  • Ensure that patient documentation is completed at each clinic visit while in screening.
  • Ensure that all medications are approved prior to initiating treatment or when changing medication regimens, such as crossover studies.
  • Accurately calculate and document BSA, Creatinine Clearance, Urine Protein: Creatinine ratio, and any other calculations or conversions required per protocol.

Additional Responsibilities:

  • Ensure that follow-up appointments, scans, or related procedures are scheduled correctly according to protocol requirements.
  • Document appropriately when patients are removed from protocol.
  • Ensure reconsent of patients at the next scheduled visit, following availability of updated ICF, and documents process appropriately.

Requirements:

  • Knowledge of medical and research terminology.
  • Knowledge of FDA Code of Federal Regulations and GCP.
  • Knowledge of the clinical research processes.
  • At least one year of oncology experience, preferably hematology and/or transplant.
  • At least one year of experience in a research setting preferred.
  • Research Certification (ACRP or CCRP) Preferred.

Education & Experience:

  • An Associate Degree; preferably a bachelor's degree.
  • RN License.

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