Research Coordinator II - Cancer Center

Job description

Overview Clinical Research Coordinator II performs a full range of clinical research duties at a skilled level and has a working knowledge of the clinical research process and the regulations that govern it. The expectation is to perform progressively more complex and comprehensive clinical research duties with an increasing level of independence, working closely with the Principal Investigator (PI). The Clinical Research Coordinator II works under the supervision of and at the direction of the PI or their designee. They cannot perform any tasks that state or local law require a license to perform. Responsibilities: Research Operations – Occasionally requiring tasks outside of defined operating hours - May arrange and/or schedule required tests and other appointments. - Understands and supports all of aspects of the study operations (including subject management/regulatory) with oversight from the investigator or their designee. - Primarily supports subject management, such as data entry in the Clinical Trial Management System(CTMS), scanning informed consents into EMR, and supporting data entry needs of the study. - May carry out study visit tasks such as administering Quality of...