Mission
People who live with cancer – those who work to prevent it, fight it, and survive it – are at the heart of every decision we make. Bringing the most innovative medical minds together with the most passionate caregivers in their communities, we are transforming care and personalizing treatment. Through clinical excellence and cutting-edge research, SCRI is redefining cancer care around the world.
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.
You will review the study design and inclusion/exclusion criteria with physician and patient.
You will ensure the protection of study patients by verifying informed consent procedures and adhering to protocol requirements.
You will use the protocol as the only tool to screen, treat, and follow patients.
You will complete and document screening/eligibility accurately.
You will complete and document the informed consent process accurately and has all parties sign/date as required, including HIPAA Authorization.
You will accurately complete and submit on-study forms within two weeks of enrollment.
You will ensure that patient documentation is completed at each clinic visit while in screening.
You will ensure that all medications are approved prior to initiating treatment or when changing medication regimens, such as crossover studies.
You will accurately calculate and document BSA, Creatinine Clearance, Urine Protein: Creatinine ratio, and any other calculations or conversions required per protocol.
You will ensure that follow-up appointments, scans, or related procedures are scheduled correctly according to protocol requirements.
You will document appropriately when patients are removed from protocol.
You will ensure reconsent of patients at the next scheduled visit, following availability of updated ICF, and documents process appropriately
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 on 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
.
As part of Total Rewards, we are proud to offer a competitive compensation package. This is determined by several factors, including performance, experience and skills, equity, regular job market evaluations, and geographical markets. In addition to base pay, other compensation, such as an annual bonus or long-term incentive opportunities may be offered.
McKesson has become aware of online recruiting-related scams in which individuals who are not affiliated with or authorized by McKesson are using McKesson’s (or affiliated entities, like CoverMyMeds or RxCrossroads) name in fraudulent emails, job postings or social media messages. In light of these scams, please bear the following in mind:
McKesson Talent Advisors will never solicit money or credit card information in connection with a McKesson job application.
McKesson Talent Advisors do not communicate with candidates via online chatrooms or using email accounts such as Gmail or Hotmail. Note that McKesson does rely on a virtual assistant (Gia) for certain recruiting-related communications with candidates.
McKesson job postings are posted on our career site: .
Research Nurse • Denver, CO, USA
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