1+ months

RESEARCH COORDINATOR

University of Washington
Seattle, WA 98104

RESEARCH COORDINATOR

Req #: 174195
Department: RADIATION ONCOLOGY
Job Location: UW Medical Center - Montlake
Posting Date: 07/30/2020 
Closing Info: Open Until Filled 
Salary: Salary is commensurate with education and experience 
Limited Recruitment: Other
Shift: First Shift 
Notes: As a UW employee, you will enjoy generous benefits and work/life programs. For a complete description of our benefits for this position, please visit our website, click here.

Please note that this position has been reposted. If you have already submitted your application, you need not submit it again, as it has already been received.  

As a UW employee, you have a unique opportunity to change lives on our campuses, in our state and around the world. UW employees offer their boundless energy, creative problem solving skills and dedication to build stronger minds and a healthier world.

UW faculty and staff also enjoy outstanding benefits, professional growth opportunities and unique resources in an environment noted for diversity, intellectual excitement, artistic pursuits and natural beauty. All of which has allowed the UW to be nationally recognized as a Great College to Work For for four consecutive years.

The Department of Radiation Oncology currently has an outstanding opportunity for a RESEARCH COORDINATOR.

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

Responsibilities:
65%  
  • Guide MDs with all aspects of the development of investigator initiated studies.   Where required, assist MDs with retrospective chart review studies of their medical students.  Submit and maintain regulatory requirements of Industry Sponsored Trials.    Submit cooperative group protocols and industry sponsored protocols as required.  Must be familiar with all aspects of regulatory and compliance functions: initial submissions to SRC, IRB, CRBB/OSP as applicable, and RSO.  As mandated by IRBs; meet Annual review deadlines, meet deadlines for amendments, compliance deviation reporting, study deviation reporting, reporting of SAEs that occur with study patients, and reporting of 3rd party SAEs.
  • Maintain all required documentation for participation of all UW-affiliated medical institutions, such as investigator information, site certifications, annual accrual figures, future applications for full RTOG member status and any other procedural requirements necessary for continued participation in the RTOG and various current and/or future clinical trials.
  • Initiate/maintain compliance with all FDA and IRB regulations and documentation requirements for each participating UWMC-affiliated institution.
  • Establish and maintain contact with MD(s) and patients regarding protocol requirements (to maintain adherence to protocol) during work up, enrollment, treatment, and long term follow up.

    15%   
  • Implement research protocols by writing and maintaining SOPs to maintain Investigator and Patient compliance.  Monitoring patient adherence to the protocol by providing compliance calendars, study calendars.  Take action to correct problems such as deviation from protocol requirements (and report deviations per IRB requirements).
  • Establish and maintain contact with MD(s) and patients regarding protocol requirements (to maintain adherence to protocol) during work up, enrollment, treatment, and long term follow up.
  • Catalog and document all designated clinical trial protocols currently accruing at UW-affiliated sites, and to update clinicians about other new/available clinical trial protocols.

    10%
  • Abstract data from clinical records and submit data per the sponsors requirements; review, maintain and meet all requirements of SOPs to maintain audit readiness.
  • Collect all case report forms, patient charts, radiographs, pathology specimens, and other clinical data pertinent to successful participation in clinical trials, as mandated by study protocols.

    5%  
  • Review of CRBB charges; ensure correct charges go to study as required.
  • Catalog and document CRBB review of charges to protocols as needed.

    5%  
  • Administer Neurocognitive Tests and Quality of Life Questionnaires or other tests per individual protocol requirements.
  • Provide assistance with auditing process from outside agencies as needed.
  • Perform related duties as required. 

    Minimum Requirements:
  • Bachelor's Degree in Biology or other related science/medical or Health Information Management AND two years experience in program management of a research project OR equivalent education and experience.
  • Must have worked in previous positions that require excellent organizational and communication skills in medical or related field and have some knowledge of regulatory requirements as it applies to research.

    Desired:
  • Certification in SoCRA, ACRP.  Previous work in research study coordination or experience working in an IRB or experience with working in CRBB. 

    Condition of Employment:
    This position may be required to work off site at any or all of the participating UW-affiliated sites.  In addition to the normal work hours, this position must be willing to work evenings, weekends, and to potentially attend the semi-annual NRG (RTOG) national group meetings and other such meetings as may be required by protocol sponsors

    Application Process:
    The application process for UW positions may include completion of a variety of online assessments to obtain additional information that will be used in the evaluation process.  These assessments may include Work Authorization, Cover Letter and/or others.  Any assessments that you need to complete will appear on your screen as soon as you select Apply to this position. Once you begin an assessment, it must be completed at that time; if you do not complete the assessment you will be prompted to do so the next time you access your My Jobs page.  If you select to take it later, it will appear on your "My Jobs" page to take when you are ready. Please note that your application will not be reviewed, and you will not be considered for this position until all required assessments have been completed.
  • Committed to attracting and retaining a diverse staff, the University of Washington will honor your experiences, perspectives and unique identity. Together, our community strives to create and maintain working and learning environments that are inclusive, equitable and welcoming.

    The University of Washington is a leader in environmental stewardship & sustainability, and committed to becoming climate neutral.

    The University of Washington is an affirmative action and equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, national origin, age, protected veteran or disabled status, or genetic information.

    To request disability accommodation in the application process, contact the Disability Services Office at 206-543-6450 / 206-543-6452 (tty) or dso@uw.edu.


    Categories

    Posted: 2020-07-31 Expires: 2020-10-17

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    RESEARCH COORDINATOR

    University of Washington
    Seattle, WA 98104
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