Research Nurse Hematology Oncology Liaison

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 the Hematology Oncology Research Nurse Liaison your primary responsibility is to screen, enroll and follow study subjects while they are in the inpatient / outpatient setting of the facility, ensuring protocol compliance and providing close monitoring while subjects are on study. You are responsible for all data collection, source documentation and submission of adverse events while research patients are either in the inpatient or outpatient departments of the facility.You will partner and collaborate with the facility inpatient / outpatient teams to ensure continuity of the research activities.

• You will attend applicablesite initiated visits(SIVs).
• You will provide initial and amended protocol education specific to the inpatient and outpatient teams.
• You will be the liaison between Sarah Cannon and facility outpatient and inpatient staff.
• You will be the main Sarah Cannon contact for facility outpatient and inpatient teams.
• You will provide daily assessment of study patients in the facility outpatient and inpatient setting, i.e. AEs, Concomittant medications, other specific protocol requirements.
• You will provide discharge orders to patient when leaving the facility outpatient and inpatient setting and ensure connectivity back to Sarah Cannon team.
• You will ensure follow-up appointments, scans, or related procedures are scheduled correctly according to protocol requirements during the discharge of a patient from the facility.
• You will provide regular patient updates / reports to Sarah Cannon when patients are in the facility outpatient or inpatient setting.
• You will collaborate with Centennial Medical Center (CMC)on study specific order sets.
• You will attend required meetings to provide patient updates and plan of care.
• You will work with Sarah Cannon and facility leadership to create, establish, monitor, and assess best practices and processes.
• You will build and maintain strategic relationships with physicians, Sarah Cannon and facility leadership.
• You will attend facility hospital review board.
• You will attend facility Blood Cancer monthly operating report(MOR).
• You will coordinate the flow of care across the various disciplines of Sarah Cannon and facility.
• You will support enrolling patients onto clinical trials through recruitment, screening, enrollment, treatment and follow-up of eligible participants according to protocol requirements.
• You will ensure the protection of study patients by verifying informed consent procedures and adhering to protocol requirements.
• You will ensurereconsent of patients at the next scheduled visit, following availability of updated ICF, and documents process appropriately.
• You will maintain patient confidentiality according to ethical and legal requirements.

You should have for this position :

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.