McKesson
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 become part of one of the largest community‑based cancer programs that advanced oncology treatments and improve outcomes for patients worldwide. We seek mission‑driven candidates who want to fight cancer and make a difference in patients’ lives 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 innovative minds with passionate caregivers together in their communities, we transform care and personalize treatment. Through clinical excellence and cutting‑edge research, SCRI is redefining global cancer care.
Responsibilities
Screen, enroll, and follow oncology research study subjects while ensuring protocol compliance.
Collect and document all study data, prepare source documentation, and submit adverse event reports.
Recruit patients, perform eligibility screening, and obtain informed consent in accordance with protocol requirements.
Attend weekly study status teleconferences and monthly staff meetings.
Maintain protection of study patients by timely adherence to protocol requirements and regulations.
Complete inclusion/exclusion forms, enrollment forms, and other protocol‑specific tools (e.g., medication forms, quality‑of‑life questionnaires, vital‑sign sheets).
Calculate body‑surface area, creatinine clearance, urine protein:creatinine ratio, and other conversions as required by protocol.
Document and report serious adverse events to the Safety Department within required timelines.
Perform study‑medication ordering, ensuring physician or nurse‑practitioner sign‑off and registrar approval for antiemetics and other agents.
Manage study medication orders, BSA calculations, and other patient‑specific documentation.
Qualifications
Associate of Nursing Degree; preferably Bachelor of Nursing Degree.
Knowledge of medical and oncology research terminology and federal regulations (GCP).
At least one year of clinical nursing experience.
At least one year of clinical research experience preferred.
At least one year of oncology nursing experience preferred.
Interested candidates should submit their application through https://www.scri.com/careers/. Applications will be accepted through February 10, 2026.
We are 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
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 become part of one of the largest community‑based cancer programs that advanced oncology treatments and improve outcomes for patients worldwide. We seek mission‑driven candidates who want to fight cancer and make a difference in patients’ lives 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 innovative minds with passionate caregivers together in their communities, we transform care and personalize treatment. Through clinical excellence and cutting‑edge research, SCRI is redefining global cancer care.
Responsibilities
Screen, enroll, and follow oncology research study subjects while ensuring protocol compliance.
Collect and document all study data, prepare source documentation, and submit adverse event reports.
Recruit patients, perform eligibility screening, and obtain informed consent in accordance with protocol requirements.
Attend weekly study status teleconferences and monthly staff meetings.
Maintain protection of study patients by timely adherence to protocol requirements and regulations.
Complete inclusion/exclusion forms, enrollment forms, and other protocol‑specific tools (e.g., medication forms, quality‑of‑life questionnaires, vital‑sign sheets).
Calculate body‑surface area, creatinine clearance, urine protein:creatinine ratio, and other conversions as required by protocol.
Document and report serious adverse events to the Safety Department within required timelines.
Perform study‑medication ordering, ensuring physician or nurse‑practitioner sign‑off and registrar approval for antiemetics and other agents.
Manage study medication orders, BSA calculations, and other patient‑specific documentation.
Qualifications
Associate of Nursing Degree; preferably Bachelor of Nursing Degree.
Knowledge of medical and oncology research terminology and federal regulations (GCP).
At least one year of clinical nursing experience.
At least one year of clinical research experience preferred.
At least one year of oncology nursing experience preferred.
Interested candidates should submit their application through https://www.scri.com/careers/. Applications will be accepted through February 10, 2026.
We are 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