Oncology Research Nurse

Screen, enroll and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study.

• Screen, enroll and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study.
• 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.
• 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.

• 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

• Medical, Dental, and Vision
• Health Spending Accounts
• Flexible Spending Accounts
• 401(k) (U.S.)
• Pension (Canada)
• Employee Stock Purchase Plan
• Mental Health Programs
• Flexible Schedules
• Paid Time Off
• Wellness Program
• Education Reimbursement
• Volunteer Opportunities
• Flexible Work Environment

Sarah Cannon Research Institute (SCRI) is one of the world’s leading oncology research organizations conducting community-based clinical trials.