Research Nurse - Enrollment

About the role

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 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 reconsent of patients at the next scheduled visit, following availability of updated ICF, and document the process appropriately.

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).
• 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. Focused on advancing therapies for patients over the last three decades, SCRI is a leader in drug development. In 2022, SCRI formed a joint venture with former US Oncology Research to expand clinical trial access across the country. It 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. SCRI’s research network brings together more than 1,300 physicians who are enrolling patients into clinical trials at more than 200 locations in 20+ states across the U.S.

Benefits

We care about the well-being of the patients and communities we serve, and that starts with caring for our people. That’s why we have a Total Rewards package that includes comprehensive benefits to support physical, mental, and financial well-being. Our Total Rewards offerings serve the different needs of our diverse colleague population and ensure they are the healthiest versions of themselves. For more information regarding benefits through our parent company, McKesson, please visit their benefits page.

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.

Pay

The salary range for this position is $83,000 - $100,000 annually.