RESEARCH COORDINATOR, RADIATION ONCOLOGY: CLINICAL TRIALS

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Provide professional-level support for clinical research studies open in Radiation Oncology; assist in protocol development, support investigativer procedures, assist in implementing protocols, and meet reporting requirements of the Scientific Review Committee (SRC), Institutional Review Boards at Fred Hutch and University of Washington (IRBs), Clinical Research Budget and Billing (CRBB), Office of Sponsored Programs (OSP) and Industry Sponsors and National Cancer Institute (NCI)

Independently, process and coordinate the operations of research studies.  This requires the knowledge and skills specific to conducting research protocols.  Assist investigators with submission of research studies to SRC, IRG, CRBB, and the Radiation Safety Office (RSO) to meet all regulatory and compliance submissions involving editing of investigator initiated protocols and consent forms as well as submission of NCI cooperative group protocols and industry protocols.  Set up and implementation of SOPs as needed to meet the requirements of and adherence to protocols.

The impact to the University will be that all Radiation Oncologists in the Department of Radiation Oncology will receive support in opening and running their investigator initiated and industry trials in a more efficient and timely manner while continuing to support cooperative group trials through the National Cancer Institute Grant.

DUTIES AND RESPONSIBILITIES