Research Nurse

No detailed description available.

• screen, enroll and follow study subjects ensuring protocol compliance and close monitoring while the subjects are on study.
• support enrolling patients onto clinical trials through recruitment, screening, enrollment and follow up of eligible subjects according to protocol requirements.
• ensure the protection of study patients by timely adherence to protocol requirements and compliance.
• review the study design and inclusion and exclusion criteria with physician and patient.
• complete and document screening and eligibility accurately.
• complete and document the informed consent process accurately and have all parties fully execute the document including HIPAA Authorization.
• complete the inclusion and exclusion form and standard enrollment form.
• accurately complete and submit the on-study forms within two weeks of enrollment for investigator-initiated protocols.
• ensure that patient documentation is completed at each clinic visit while in screening.
• ensure that all medications are approved by the registrar prior to initiating treatment or when changing medication regimens, such as crossover studies.
• accurately calculate and documents the BSA, creatinine clearance, urine protein:creatinine ratio or any other conversions needed per protocol.
• ensure that follow-up appointments, scans, or any related procedures are scheduled correctly according to protocol requirements.
• inform and document appropriate SCRI and clinic personnel when patient comes off study.

• 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 preferred
• 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)
• Pension
• 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.