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About the Role
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. You will be responsible for all data collection, source documentation, and recording of adverse events.
Responsibilities
- Screen, enroll, and follow study subjects, ensuring protocol compliance and close monitoring.
- Collect data, maintain source documentation, and record adverse events.
- Recruit, screen, enroll, treat, and follow eligible participants according to protocol requirements.
- Review 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 sole tool to screen, treat, and follow patients.
- Accurately complete and document screening/eligibility.
- Accurately complete and document the informed consent process, ensuring all parties sign/date as required, including HIPAA Authorization.
- Accurately complete and submit on-study forms within two weeks of enrollment.
- Ensure patient documentation is completed at each clinic visit during screening.
- Ensure all medications are approved prior to initiating treatment or when changing medication regimens.
- Accurately calculate and document BSA, Creatinine Clearance, Urine Protein: Creatinine ratio, and any other calculations or conversions required per protocol.
- Ensure 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 process appropriately.
Requirements
- 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
Experience Level
- At least one year of oncology experience
- At least one year of experience in a research setting
Education Level
- Associate Degree
- Bachelor’s Degree
- RN License
Salary/Compensations
- Competitive compensation package determined by performance, experience, skills, equity, 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.
Benefits
- Comprehensive benefits to support physical, mental, and financial well-being.
About the Company
- 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.
Equal Opportunity
- 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.