Research Nurse Hematology Oncology Liaison

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 responsiblefor all data collection, source documentationand 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 continuityof the research activities.

• You will attend applicable site 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 ensure reconsent 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:

• An Associate Degree, preferably a Bachelor's Degree
• License to practice as a Registered Nurse
• Research certification (ACRP or CCRP) is preferable
• Knowledge of medical and research terminology
• Knowledge of FDA Code of Federal Regulations and GCP
• Public presentation skills
• A minimum of one year of oncology experience, preferably hematology/oncology and/or transplant
• Experience in clinical research setting is preferred