Research Nurse

OneOncology•Chattanooga, TN

1d•Onsite

About The Position

Tennessee Oncology, one of the nation’s largest, community-based cancer care specialists, is home to one of the leading clinical trial networks in the country. Established in 1976 in Nashville, Tennessee Oncology’s mission is to provide access to high-quality cancer care and the expertise of clinical research for all patients, at convenient locations within their community and close to their home. The organization is committed to advancing both the science of detection and targeted treatments, and to making these advances available to every patient. As the Research Nurse for Tennessee Oncology Greco Hainsworth Center for Research, this role is critical in advancing oncology research by ensuring the successful execution of clinical trials. Responsibilities include screening, enrolling, documenting, and monitoring study subjects, ensuring strict protocol compliance and delivering exceptional patient care.

Requirements

Strong attention to detail and organizational skills.
Ability to work independently while collaborating effectively with a multidisciplinary team.
Knowledge of medical and research terminology
Knowledge of the FDA Code of Federal Regulations and GCP
Knowledge of the clinical research processes
An Associate Degree, preferably a bachelor’s degree
RN License
At least one year of oncology experience

Nice To Haves

At least one year of experience in a research setting is preferred.
Research Certification (ACRP or CCRP) Preferred

Responsibilities

Enroll patients in clinical trials through recruitment, screening, enrollment, treatment, and follow-up of eligible participants according to protocol requirements.
Provide thorough education about study requirements and expectations.
Complete and document the informed consent process accurately, ensuring all parties sign and date as required, including obtaining HIPAA Authorization.
Obtains and maintains informed consent of each patient for the duration of a study.
Review the study design and inclusion/exclusion criteria with the physician and the patient.
Complete and submit on-study forms within required timelines.
Maintain accurate and detailed source documentation, including study visits findings, and outcomes.
Screen all new patients or patients returning to the office with scan results and document appropriately on patient tracking logs.
Monitor subjects throughout the study, ensuring protocol compliance and patient safety.
Ensure that all medications are approved before initiating treatment or changing medication regimens, such as crossover studies.
Dispense oral investigational products to study participants and provide guidance to ensure compliance with medication regimens.
Accurately calculate and document BSA, Creatinine Clearance, Urine Protein: Creatinine ratio, and any other calculations or conversions required per protocol.
Ensure that follow-up appointments, scans, or related procedures are scheduled correctly per protocol requirements.
Record and report adverse events according to study protocols and regulatory requirements.
Document appropriately when patients are removed from the protocol.
Ensure reconsent of patients at the next scheduled visit, following the availability of the updated ICF, and document the process appropriately.
Provide patient education and medical information to study patients to ensure understanding of proper medication dosage, administration, and disease treatment.
Maintains medication inventory and reconciliation.
Collaborate with the clinical research team to ensure the timely completion of study-related tasks and reporting.
Liaison between study participants, investigators, and the research team to address questions and concerns.
Float to other research Tennessee Oncology clinics as needed.