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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.
SMMART is the cutting edge flagship program of the Knight Cancer Institutes new Precision Oncology program. Our name stands for Serial Measurements of Molecular and Architectural Responses to Therapy and we are designed to change the way we approach cancer research and treatments. SMMART has the ambitious goal of developing innovative cancer treatment regimens that last longer (are more durable) and allow better quality of life (are more tolerable) for patients with cancer at all stages. Through comprehensive and longitudinal analysis the SMMART program evaluates each patients individual cancer tumor with the mission to understand why standard therapies often stop working and to develop novel combinations that may stop cancers from becoming resistant to cancer .
SMMART is a highly adaptive fastpaced intense research environment. We work to support the conduct of translational clinical research aimed at improving the lives of people and families with cancer by applying innovative strategies for cancer prevention screening diagnosis and treatment that is uniquely tailored to each patient. We support this model through proactive high quality and efficient study management in compliance with federal regulations and local policies and procedures. We navigate the complex world of oncology and clinical studies and work with a very vulnerable and sick population.
We are seeking a motivatedClinical Research Coordinator (TI Senior Clinical Research Assistant)who is eager to learn and interested in joining our highly dynamic team whose goal is to change how we attack cancer.
Every Knight Cancer employee is expected to embody our guiding principles:
The SMMART Clinical Research Coordinator (TI Senior Clinical Research Assistant) will be responsible for leading the coordination duties and efforts associated with direct patient management for our SMMART clinical research trials and/or maintaining close collaboration with our disease team partners to comanage participants as required by the study. This position will have direct patient contact (inperson and remotely via phone) may process and collect biological samples such as biopsy tissue and blood and may perform other noninvasive testing such as ECGs as directed by a clinical trial. As a senior Clinical Research Coordinator this position may also assist the management team in providing guidance and support training to juniorlevel Clinical Research Coordinators once fully onboarded.
This position will collaborate closely with the SMMART regulatory and data teams as well as the SMMART translational research team to ensure patient participation activities are adhered to per clinical trial requirements and guidelines. Key duties may include but are not limited to: performing consent discussions with participants verification of participant eligibility maintenance of participant charts and forms data entry maintaining appropriate source documentation and will frequently submit orders for research tests and procedures with heavy use of EPIC. This position may coordinate collections procurement and shipping of biological specimens may assist in the development of biospecimen collection SOPs and workflows develop and maintain SMMART coordinator toolkits and resources order research study and supplies and may assist manager with verification of patient billing when queried. For collaborative studies this position will also assist as a liaison for collaborative disease team coordinators to field questions and ensure conduct of the studys schedule of events are followed appropriately.
Level of research responsibility for this positionrequires general supervision. This position will be expected to complete responsibilities with moderate oversight to perform tasks and requires increased innovation and problem solving understanding of protocol requirements and adherence and data management.
This Clinical Research Coordinator is also responsible for assisting in the continuing education of physicians residents interns nurses and other related personnel with regards to knowledge of SMMART clinical trials and activities. The CRC always promotes the mission of the Knight Cancer Institute through our professional standards of customer service reliability productivity professionalism accuracy timeliness and problemsolving.
Education and experience:
Required Competencies:
Apply here online. Please be sure to upload a cover letter and resume or CV.
Every Knight Cancer employee is expected to embody our guiding principles:
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Senior IC
Full-Time