A Clinical Research Coordinator (CRC) II-III is a senior-level coordinator that works under the supervision of the Clinical Research Program Manager and is responsible for a portfolio of complex interventional clinical protocols. The CRC II-III will facilitate the planning, coordination, and implementation of Community Clinical Oncology Program (CCOP) and industry-sponsored studies involving human subjects. The CRC II-III will have daily interaction with PI, study staff, pharmaceutical sponsors, physicians, and other health care personnel as part of a cross-functional team working within Virginia Mason Medical Center and Benaroya Research Institute. The incumbent will be required to perform responsibilities with high level of independence.
Subject care requirements may include:
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, citizenship, disability or protected veteran status.