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Research Coordinator

UW Medical Center

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Job Details

Location: Astronomy by Day (and Other Oxymorons), 4th Avenue, Central Business District, First Hill, Seattle, King County, Washington, 98104, USA Posted: May 02, 2024

Job Description

RESEARCH COORDINATOR

Req #: 233603 Department: DEPARTMENT OF MEDICINE: HEMATOLOGY & ONCOLOGY Job Location: Seattle - Other Posting Date: 05/01/2024 Closing Info: Closes On 05/08/2024 Salary: $6,000 - $7,084 per month Other Compensation: Limited Recruitment: Open to UW Employees only
If you are a UW employee and would like to be considered for this position, please login to your UW employee profile to apply. Shift: First Shift Benefits: 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. 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.
The purpose of this position is to promote the research objectives of the Division of Hematology. This position works with Division of Hematology faculty to facilitate investigator-initiated and industry-sponsored clinical trials.
This position is constantly required to integrate information from multiple sources to ensure that all research proposals meet the requirements of the University, the Food and Drug Administration, the National Institutes of Health and the study sponsor. This position develops procedures that ensure that all research meets or exceeds these requirements while expeditiously furthering the research objectives of the Division of Hematology. There are multiple resources available within the University system (e.g. Grant and Contract Services, Institutional Review Board, Office of Industry Relations) to help in this process, but ultimately, the work must be done independently and in a resourceful manner to expedite the Division’s research objectives. This position is also responsible for organizing and facilitating sponsor-initiated, FDA-initiated, and institution-initiated audits of study data. Finally, this position interacts with representatives from federal and state agencies, foundations, pharmaceutical companies, health care providers and cancer patients in a manner that well-represents the University of Washington and its associated institutions (FHCRC and SCCA).
The mission statement of the University of Washington Medical Center states that the Medical Center serves as a research resource, providing an environment in which clinical research may be conducted. This position is essential to that mission. This position provides significant contributions to research development, implementation and analysis for the Division of Hematology. It is responsible for overseeing the management of clinical trials.
This position must be able to work independently under administrative direction on multiple research projects; at times, without the benefit of written policies or procedures, while concurrently helping to create best practices moving forward. This position requires daily interaction with sponsors, physicians, the U.S. Food and Drug Administration, other health care personnel (e.g. nurses, patient care coordinators, insurance companies), and patients. Up to 15 projects will be in progress simultaneously, with the expectation of additional projects in the future.
DUTIES AND RESPONSIBILITIES
Protocol Development and Management, and Regulatory - 45%
  • Write informed consent documents that clearly describe the nature and risks of the research project in language that is easily understandable to the individual patient.
  • Timely and appropriate reporting of Adverse Events and Serious Adverse Events to sponsors and review boards to ensure compliance to protocol and FDA requirements.
  • Work with multiple UW, SCCA, and Fred Hutchinson Cancer Research Center (FHCRC) groups (e.g. UW Grant and Contract Services, UW Human Subjects Review Committee, UW and SCCA Radiation Safety Committee, UW and FHCRC Biosafety Committee, SCCA Research Implementation Office, and UWMC General Clinical Research Center) to ensure timely implementation of each research project.
  • Protocol Management – Independently develop and implement research project policies and procedures that meet research objectives and that ensure compliance with all aspects of Federal Drug Administration (FDA) and National Institutes of Health (NIH) regulations pertaining to clinical research in human subjects (e.g. investigator financial disclosure requirements of the FDA).
  • Design, develop, document and maintain policies and procedures for protocol registration and implementation to ensure that research execution meets good clinical practice guidelines.
  • Design, create and revise research instruments (e.g. case report forms) as necessary to ensure quality data that correlates with research objectives.
  • Design, document and implement procedures for protocol audits to assure protocol compliance and to ensure research data quality.
    Study Subject Management – 40%
  • Take action to correct problems such as deviation from protocol requirements to ensure research quality.
  • Ensure that projects are executed successfully and completed within needed time frames to meet research objectives.
  • Process labs for clinical trials, including collecting, centrifuging and aliquoting specimens, and ship specimens in accordance with federal and institutional biologics shipping regulations.
  • Patient Management - Ensure protocol compliance by managing patient appointments and coordinating with patient’s clinical providers (e.g. physicians, physician assistants, and nurses) to collect reliable and accurate data.
  • Ensure patient safety while participating in clinical trials by monitoring patients and interacting closely with patient’s clinical providers.
  • Initiate and maintain communication with outside physicians who refer patients to UWMC for Hematologic clinical trials.
    Analysis and Reporting – 15%
  • Analysis and Reporting – Prepare interim reports for principal investigators, industry sponsors and Institutional Review Board to ensure that each project is moving toward timely completion.
  • Prompt completion of electronic data capture systems and electronic case report forms.
  • Timely resolution of queries and questions from industry sponsors, contract research organizations, institutional groups and our affiliates.
  • Other duties as assigned
    MINIMUM REQUIREMENTS
  • Bachelor's Degree in related field.
  • Two years experience.
  • Equivalent education/experience will substitute for all minimum qualifications except when there are legal requirements, such as a license/certification/registration.
    ADDITIONAL REQUIREMENTS
  • Knowledge of HIPAA regulations.
  • Knowledge of FDA and GCP (Good Clinical Practice).
  • Strong attention to detail and ability to multi-task, organize and prioritize projects.
  • Experience working in inpatient/outpatient research setting.
  • Excellent written and verbal communication skills, experience with Microsoft Office.
  • Applicants selected for this position who have not already completed the training for clinical research involving human subjects will be required to complete it within 30 days of hire.
    DESIRED QUALIFICATIONS
  • Previous experience working with Hematology patients.
  • CCRC or CCRP endorsement
    CONDITIONS OF EMPLOYMENT
  • This position requires a flexible work schedule. Stringent deadlines from sponsors and faculty for protocol implementation and data collection may require overtime. Integrating required elements of research into complex patient schedules (e.g collecting and processing multiple blood specimens for pharmacokinetic sampling) may also require occasional overtime.
  • Must be available to enroll patients and maintain email/pager contact with 24/7 availability. Some evening and weekend travel to study meetings and sites may be required.
  • This position is located in a clinical research environment located at the Seattle Cancer Care Alliance on the Fred Hutchinson Cancer Research Center campus and requires the physical ability to get between offices, clinic and other facilities, up to 1-mile distance.
    Application Process: The application process 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 access 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 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 or [email protected] .

    Applicants considered for this position will be required to disclose if they are the subject of any substantiated findings or current investigations related to sexual misconduct at their current employment and past employment. Disclosure is required under Washington state law .

    Open to UW Employees only
    If you are a UW employee and would like to be considered for this position, please login to your UW employee profile to apply.

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