The OHSU Knight Cancer Institute, known as one of the pioneers in personalized cancer medicine, is an international leader in research and cancer treatment. Driven by its mission to end cancer as we know it, the institute is building upon its expertise in targeted treatments to advance the early detection of cancer when the disease is most treatable. Cancer Early Detection Advanced Research Center (CEDAR) is a highly collaborative institution within the OHSU Knight Cancer Institute. At CEDAR our mission is to detect and stop lethal cancers at the earliest stage because early detection saves lives. This is an ambitious goal, one that requires novelty, creativity, and innovation. We conduct groundbreaking translational cancer research to help people maintain a high quality of life and reduce cancer mortality, to create a global early detection community, and to have a positive impact on the Oregon economy. Our clinical trials are cutting edge and laser focus on the exciting and rapidly evolving area of cancer early detection. CEDAR is committed to increasing the diversity of the campus community. We are dedicated to promoting inclusion and multiculturalism to build a successful organization by having outstanding researchers of diverse backgrounds work together.
Every Knight Cancer employee is expected to embody our guiding principles:
The CEDAR Clinical Research Coordinator is responsible for the overall management of early detection clinical trials at Bay Area Hospital and Southern Oregon. This position is located in Coos County, Oregon, requiring in-person work at Bay Area Hospital Cancer Center, with limited work from home opportunities during the week. This includes working closely with the regulatory and cordination team in Portland remotely to assist in the completion of all regulatory documentation required by the OHSU IRB and sponsor, creation of study calendars and flow charts, assisting in the verification of patient eligibility, development of data collection instruments and consent forms, data entry, assurance of conduct of protocol in accordance with applicable NCI and FDA guidelines, maintenance of study patient records and source documentation, coordinating orders and study drug with the clinical team, ensuring that patient billing is accurate and assisting manager and financial team in verifying appropriate clinical trial billing. The study coordinator will have direct patient contact and process biological samples. The study coordinator will also assist with community outreach to reach a diverse population for recruitment and support the Bay Area Hospital (BAH) subsite in recruitment and enrollment.
Duties include:
Participant Coordination
Clinical Trial coordination
Apply online. Please be sure to upload a Cover Letter and Resume/CV.
We offer a variety of benefits on top of joining a thriving organization:
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