Oncology Research Nurse

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 the most innovative medical minds together with the most passionate caregivers in their communities, we are transforming care and personalizing treatment. Through clinical excellence and cutting-edge research, SCRI is redefining cancer care around the world.

As an Oncology Research Nurse your primary responsibility is to screen, enroll and follow oncology research study subjects ensuring protocol compliance and close monitoring while patients are on the study. You are responsible for all data collection, source documentation and submission of adverse experience reports.

• You will support enrolling patients onto clinical trials through recruitment, screening, enrollment and follow up of eligible subjects.
• You will ensure the protection of study patients by timely adherence to protocol requirements and compliance
• You will attend weekly study status teleconference and monthly staff meetings
• You will be familiar with the protocols on which the patients are enrolled, screen, treat, and follow patients
• You will review the study design and inclusion / exclusion criteria with physician and patient.
• You will complete and document screening / eligibility and consent accurately and have all parties fully execute the document including HIPAA Authorization
• You will complete the inclusion / exclusion form and standard enrollment form accurately and assess the patient and document findings at each clinic visit while on protocol
• You will document all specific tools required by the protocol (i.e. oral medication forms, pill count diaries, quality of life questionnaires, neuro exams, vital signs sheets, times of PK draws, etc.)
• You will screen every new patient or patient returning to office with scan results and document appropriately on the patient tracking logs
• You will complete the study medication order form and have the physician or nurse practitioner sign orders prior to treatment and ensure that all medications, including antiemetics, are approved by the registrar prior to initiating treatment or when changing medication regimens, such as crossover studies
• You will calculate the BSA, creatinine clearance, urine protein : creatinine ratio or any other conversions needed per protocol
• You will obtain completed and signed waivers prior to submitting forms to enrollment coordinator for investigator-initiated protocols and re-consent patients in a timely manner and document process appropriately
• You will accurately complete and submitfollow-up serious adverse event (SAE) report to the Safety Department within the time frame allotted by the Regulatory Department.

You should have :

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.