Overview

Do you want to be a part of improving the healthcare of United States Veterans through meaningful work in a collaborative environment? The Department of Veterans Affairs (VA) Cooperative Studies Program (CSP) is a nationally renowned program of epidemiology and clinical trial research centers that produce innovative and effective solutions to Veteran and national healthcare problems through high quality multi-site research studies.
The Seattle Network of Dedicated Enrollment Sites is looking to hire a full-time employee that will provide research coordination for multi-site clinical trials at VA Puget Sound. The Research Study Coordinator will work closely with the Seattle NODES Research Program Manager, Center Directors and CSP study teams to assure the success of their studies. The Seattle NODES is 1 of 21 NODES within CSP.
This position is based in Seattle, WA.
Key Duties:
• Under the direction of the NODES Research Program Manager, participates in all aspects of conducting clinical research. Includes, but is not limited to feasibility assessments, screening/recruiting potential study participants, obtaining informed consent, enrollment, randomization, scheduling research appointments, data collection, study procedures, study surveys, collection/processing of biospecimens, reporting study adverse events/side effects and completing appropriate study documentation for multiple research studies in-person or over the telephone.
• Prepares study materials including, but not limited to, regulatory paperwork, informed consent document, case report forms (CRFs), enrollment logs, participant reimbursement, and drug/device accountability logs.
• Establishes and organizes study files, including but not limited to, regulatory binders, study specific source documentation and other materials.
• Works with the NODES Program Manager to manage the day-to-day activities of the portfolio of research studies including problem solving, communication and protocol management.
• Creates and maintains complex research databases and manages spreadsheets for data tracking and other project management tracking tasks.
• Independently responds to general inquiries from study participants, research and R&D administration staff, and other stakeholders. Independently drafts correspondence and general communications regarding the center.
• Assists in the development and implementation of clinical research standard operating procedures and policies, quality assurance and quality control activities.
• Attends study and center meetings, as required.

Provides training and technical guidance to research team members regarding regulations, policies, and procedures applicable to the conduct of the research.

Stays up to date on federal rules and regulations and VA, ORD, CSP, and local VA policies and procedures as they relate to research, privacy, and data sharing; oversees NODES
regulatory processes; assists with responses to complex and nuanced regulatory inquiries, including responding to research incidents and preparing for audits

Performs other related duties as outlined in research protocols, and other duties as assigned.
Qualifications:
Required:

Education Requirements:
o
BA/BS in a scientific- or health-related field and 2-3 years of work experience in clinical, epidemiological, or health services research required OR
o
Master’s or higher degree in a scientific- or health-related field required and 1-2 years of work experience in clinical, epidemiological, or health services research preferred

Excellent communication and interpersonal skills with the ability to collaborate with a diverse group of researchers and staff

Strong attention to detail and organizational skills

Solid problem-solving and critical thinking skills

Excellent time management skills

Ability to adapt to changing priorities and timelines

Proficiency in Microsoft Word, Excel, PowerPoint, and Outlook
Preferred:

Experience coordinating and executing large-scale research studies

Institutional knowledge of VA and/or CSP research operations

Knowledge of REDCap and Microsoft Access

Experience working with underserved and/or Veteran populations
There may be travel opportunities for national CSP research meetings and to regional sites.
Application Information
All positions are based in Seattle, WA and all candidates must be U.S. citizens. Selected candidates’ education and experience will be evaluated by Human Resources to determine if they meet the criteria for the targeted GS-9. The General Schedule (GS) salary table for Seattle can be found on the Office of Personnel Management website at opm.gov.
To apply, please send a cover letter and resume to Julieann.Marshall@va.gov.
Applications will be accepted until the position is filled; however, materials received by 2/16/2026 will be considered first.
For more information about the CSP NODES, please see Network of Dedicated Enrollment Sites (NODES) – VA Cooperative Studies Program (CSP).

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About Seattle Epidemiologic Research and Information Center (ERIC), Department of Veterans Affairs (VA)

All positions are based in Seattle, WA and all candidates must be U.S. citizens. Selected candidates’ education and experience will be evaluated by Human Resources to determine if they meet the criteria for the targeted GS-9. The General Schedule (GS) salary table for Seattle can be found on the Office of Personnel Management website at opm.gov.
To apply, please send a cover letter and resume to Julieann.Marshall@va.gov.
Applications will be accepted until the position is filled; however, materials received by 2/16/2026 will be considered first.
For more information about the CSP NODES, please see Network of Dedicated Enrollment Sites (NODES) - VA Cooperative Studies Program (CSP).