University of Washington
Job Description
BThe Department of Radiation Oncology has an outstanding opportunity for a full-time Data Coordinator. The purpose of this position is to promote the research objectives of the department. This position works with faculty and staff to facilitate investigator-initiated, clinical registries, and clinical research studies. This position must be able to work independently under administrative direction on multiple research projects, without benefit of written policies or procedures. This position requires daily interaction with team members, and may require interaction with Sponsors, health care personnel, and patients as needed for the successful completion of research projects. Multiple projects may be in progress simultaneously, with the expectation of additional projects in the future. This position requires schedule flexibility (hybrid role) with the need to be on-site up to 5 days a week as needed for project coordination. Research occurs amongst multiple sites of practice, and may require the need to travel between sites as needed. Duties And Responsibilities
BData Coordination, Abstraction, Input, and Analysis – 70% Work independently and with study team members to obtain, abstract, and code complex clinical information from multiple sources (medical records, research records, etc.) for research subjects. Code and record said information into various study-specific data-capture systems (both electronic and paper-based). Work with sponsor representatives and research staff to review data, and resolve data queries with minimal errors. With other study team members, make judgments about the relevance of the clinical data to the research for complicated radiation oncology research subjects. Responsible for maintaining computer spreadsheets and databases for research studies. May work with study team to draft scheduling request orders to meet study protocol needs. Act on regulatory requests to assist with Honest Broker activities. BProcess Improvement/Study Data Analysis – 15% Work with the study team and other groups to develop process improvement tools. Assist in the assessment and design of tracking tools to develop standard data practices. Assist Investigators and study team members with preparation and analysis of study data for publication and grant preparation. BProtocol Coordination – 10% Collate and maintain clinical information from multiple sources into research charts, study binders, etc. Track and maintain research subject schedules based on complex protocol-specific requirements. Assist with retrieval and return of patient kits, materials, specimens, etc. Ability to learn and perform electrocardiograms (EKG) BResearch Billing – 5% May assist Research Coordinators and Assistant Director, Finance, Grants, and Contracts with the proper billing of research charges and budget development. Perform related tasks as assigned Minimum Requirements
Bachelor’s Degree in biology, psychology, public health, nursing, or related field and one year of experience with clinical trials in the medical field. Equivalent education and/or experience may substitute for minimum qualifications except when there are legal requirements, such as a license, certificate, and/or registration. Desired
Strong computer skills and competency with Microsoft Office software. Strong attention to detail and ability to multi-task, organize and prioritize multiple projects. Excellent written and verbal communication skills. Demonstrated ability to work independently, under supervision, and be a team player. Should be highly motivated and flexible, with the ability to adjust to rapidly changing priorities and new projects. Maintain positive vision, sense of humor, and professional demeanor under potentially stressful situations. Applicants selected for this position who have not already completed the training for clinical research involving human subjects will be required to complete this training. Perform varied support functions requiring knowledge and skills specific to the research study Provide preparatory support that will enable the study coordinators to effectively record subject data Ability to be flexible in a multitude of professional situations Perform related duties as needed or required Ability to maintain effective communication with study coordinators, sponsors, health care personnel, patients, and Principal Investigator’s (i.e. task completion, prioritization, size of workload) Ability to work independently and expeditiously Demonstrated understanding of medical terminology, specifically in oncology Familiarity with Epic systems Familiarity with clinical research Knowledge of University of Washington/Fred Hutch Cancer Center processes Familiarity with REDCap Compensation, Benefits And Position Details
Pay Range Minimum: $48,648.00 annual Pay Range Maximum: $60,000.00 annual For information about benefits for this position, visit https://www.washington.edu/jobs/benefits-for-uw-staff/ Shift
First Shift (United States of America) Temporary or Regular?
This is a regular position FTE (Full-Time Equivalent)
100.00% Union/Bargaining Unit
UAW Research About The UW
Working at the University of Washington provides a unique opportunity to change lives … Our Commitment
The University of Washington is proud to be 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 dso@uw.edu. 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.
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BThe Department of Radiation Oncology has an outstanding opportunity for a full-time Data Coordinator. The purpose of this position is to promote the research objectives of the department. This position works with faculty and staff to facilitate investigator-initiated, clinical registries, and clinical research studies. This position must be able to work independently under administrative direction on multiple research projects, without benefit of written policies or procedures. This position requires daily interaction with team members, and may require interaction with Sponsors, health care personnel, and patients as needed for the successful completion of research projects. Multiple projects may be in progress simultaneously, with the expectation of additional projects in the future. This position requires schedule flexibility (hybrid role) with the need to be on-site up to 5 days a week as needed for project coordination. Research occurs amongst multiple sites of practice, and may require the need to travel between sites as needed. Duties And Responsibilities
BData Coordination, Abstraction, Input, and Analysis – 70% Work independently and with study team members to obtain, abstract, and code complex clinical information from multiple sources (medical records, research records, etc.) for research subjects. Code and record said information into various study-specific data-capture systems (both electronic and paper-based). Work with sponsor representatives and research staff to review data, and resolve data queries with minimal errors. With other study team members, make judgments about the relevance of the clinical data to the research for complicated radiation oncology research subjects. Responsible for maintaining computer spreadsheets and databases for research studies. May work with study team to draft scheduling request orders to meet study protocol needs. Act on regulatory requests to assist with Honest Broker activities. BProcess Improvement/Study Data Analysis – 15% Work with the study team and other groups to develop process improvement tools. Assist in the assessment and design of tracking tools to develop standard data practices. Assist Investigators and study team members with preparation and analysis of study data for publication and grant preparation. BProtocol Coordination – 10% Collate and maintain clinical information from multiple sources into research charts, study binders, etc. Track and maintain research subject schedules based on complex protocol-specific requirements. Assist with retrieval and return of patient kits, materials, specimens, etc. Ability to learn and perform electrocardiograms (EKG) BResearch Billing – 5% May assist Research Coordinators and Assistant Director, Finance, Grants, and Contracts with the proper billing of research charges and budget development. Perform related tasks as assigned Minimum Requirements
Bachelor’s Degree in biology, psychology, public health, nursing, or related field and one year of experience with clinical trials in the medical field. Equivalent education and/or experience may substitute for minimum qualifications except when there are legal requirements, such as a license, certificate, and/or registration. Desired
Strong computer skills and competency with Microsoft Office software. Strong attention to detail and ability to multi-task, organize and prioritize multiple projects. Excellent written and verbal communication skills. Demonstrated ability to work independently, under supervision, and be a team player. Should be highly motivated and flexible, with the ability to adjust to rapidly changing priorities and new projects. Maintain positive vision, sense of humor, and professional demeanor under potentially stressful situations. Applicants selected for this position who have not already completed the training for clinical research involving human subjects will be required to complete this training. Perform varied support functions requiring knowledge and skills specific to the research study Provide preparatory support that will enable the study coordinators to effectively record subject data Ability to be flexible in a multitude of professional situations Perform related duties as needed or required Ability to maintain effective communication with study coordinators, sponsors, health care personnel, patients, and Principal Investigator’s (i.e. task completion, prioritization, size of workload) Ability to work independently and expeditiously Demonstrated understanding of medical terminology, specifically in oncology Familiarity with Epic systems Familiarity with clinical research Knowledge of University of Washington/Fred Hutch Cancer Center processes Familiarity with REDCap Compensation, Benefits And Position Details
Pay Range Minimum: $48,648.00 annual Pay Range Maximum: $60,000.00 annual For information about benefits for this position, visit https://www.washington.edu/jobs/benefits-for-uw-staff/ Shift
First Shift (United States of America) Temporary or Regular?
This is a regular position FTE (Full-Time Equivalent)
100.00% Union/Bargaining Unit
UAW Research About The UW
Working at the University of Washington provides a unique opportunity to change lives … Our Commitment
The University of Washington is proud to be 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 dso@uw.edu. 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.
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