As a Research Nurse in the Drug Development Unit 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. You should have for this position 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, 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.
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