Research Nurse

McKesson•Denver, CO

5d•$83,000 - $100,000•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 the Research Nurse your primary responsibility is to screen, enroll and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study. You are responsible for all data collection, source documentation, and recording of adverse events. You will be enrolling patients onto clinical trials through recruitment, screening, enrollment, treatment, and follow-up of eligible participants according to protocol requirements.

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
At least one year of oncology experience, preferably hematology and/or transplant.
At least one year of experience in a research setting preferred

Nice To Haves

Research Certification (ACRP or CCRP)

Responsibilities

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.
Use the protocol as the only tool to screen, treat, and follow patients.
Complete and document screening/eligibility accurately.
Complete and document the informed consent process accurately and has all parties sign/date as required, including HIPAA Authorization.
Accurately complete and submit on-study forms within two weeks of enrollment.
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.
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.