Research Nurse

It's More Than a Career, It’s a Mission. 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. Our 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. Job Overview As the Research Nurse for Blood Cancer and Bone Marrow Transplant, 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. Responsibilities Enroll patients onto clinical trials through recruitment, screening, enrollment, treatment, and follow‑up of eligible participants according to protocol requirements. 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 ensure 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 re‑consent of patients at the next scheduled visit, following availability of updated ICF, and document process appropriately. Qualifications 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. Research Certification (ACRP or CCRP) Preferred. About Sarah Cannon Research Institute Sarah Cannon Research Institute (SCRI) is one of the world’s leading oncology research organizations conducting community‑based clinical trials. SCRI has conducted more than 850 first‑in‑human clinical trials since its inception and contributed to pivotal research that has led to the majority of new cancer therapies approved by the FDA in the past decade. Equal Opportunity Employer We’re an equal‑opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. #J-18808-Ljbffr McKesson Corporation