Oncology Clinic Research Nurse

Sarah Cannon Research Institute•Nashville, TN

1d•Onsite

About The Position

Our people are the foundation of our success. By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will have the opportunity to become part of one of the largest community-based cancer programs to advance oncology treatments and improve outcomes for cancer patients across the globe. We look for mission-driven candidates who have a desire to advance the fight against cancer and make a difference in the lives of patients diagnosed with cancer every day. As a Research Nurse your primary responsibility is to follow study subjects ensuring protocol compliance and close monitoring while the subjects are on study. You will ensure the protection of study patients by timely adherence to protocol requirements and compliance. You will use the protocol as the only tool to screen, treat, and follow patients. You will ensure that patient documentation is completed at each clinic visit while in screening. You will ensure that all medications are approved by the registrar prior to initiating treatment or when changing medication regimens, such as crossover studies. You will accurately calculate and documents the BSA, creatinine clearance, urine protein:creatinine ratio or any other conversions needed per protocol. You will ensure that follow-up appointments, scans, or any related procedures are scheduled correctly according to protocol requirements. You will inform and document appropriate SCRI and clinic personnel when patient comes off study.

Requirements

An Associate Degree; preferably a Bachelor’s Degree
RN License
Knowledge of medical and research terminology
Knowledge of FDA Code of Federal Regulations and GCP
Knowledge of the clinical research processes

Nice To Haves

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

Responsibilities

Follow study subjects ensuring protocol compliance and close monitoring while the subjects are on study.
Ensure the protection of study patients by timely adherence to protocol requirements and compliance.
Use the protocol as the only tool to screen, treat, and follow patients.
Ensure that patient documentation is completed at each clinic visit while in screening.
Ensure that all medications are approved by the registrar prior to initiating treatment or when changing medication regimens, such as crossover studies.
Accurately calculate and documents the BSA, creatinine clearance, urine protein:creatinine ratio or any other conversions needed per protocol.
Ensure that follow-up appointments, scans, or any related procedures are scheduled correctly according to protocol requirements.
Inform and document appropriate SCRI and clinic personnel when patient comes off study.