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University of Washington

Research Coordinator 2

Seattle, WASalary not listedPosted yesterday

Immigration summary

Visa sponsorship

LikelyHigh confidence

This employer has recently sponsored work like this.

195 recent H-1B filings · 1 similar-role filing

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Green card sponsorship

Strong historyMedium confidence

This employer has recently sponsored green cards at scale.

25 recent certified PERM filings

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Job description

Job Description

The Department of Radiation Oncology has an outstanding opportunity for a full-time Research Coordinator.

About this Opportunity

This position needs to 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.

Key responsibilities:

55% 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), residents, fellows 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. Work in a fast paced environment, in conjunction with multi-disciplinary teams (medical oncology, radiology, laboratory, etc) to meet the clinical needs of patients while enrolled in a clinical trial.

20% Abstract data from clinical records and submit data per the sponsor’s 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.

10% Guide MDs with all aspects of the development of investigator initiated studies. Where required, assist MDs with retrospective chart review studies by their medical students. Must be familiar with all aspects of regulatory and compliance functions: initial submission 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 compliance, in conjunction with regulatory coordinator, with all FDA and IRB regulations and documentation requirements for each participating UWMC-affiliated institution.

10% 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.

5% Review of CTO, FHCC and vendor charges; ensure correct charges go to study as required. Catalog and document review of charges to protocols as needed, in conjunction with financial team.

Required Qualifications:

To be considered for this opportunity your application must demonstrate you meet both the minimum qualifications and additional qualifications listed below. Equivalent education and/or experience may substitute for minimum qualifications except when there are legal requirements, such as a license, certification, and/or registration.

Minimum Qualifications:

  • Bachelor’s Degree in biology, other related science/medical or Health Information Management
  • Two years of relevant patient-facing clinical research experience in a clinical setting.
  • “Applicants who do not meet these qualifications WILL NOT be forwarded to the Hiring Manager.”

Preferred Qualifications:

  • 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.
  • Certification on SoCRA, ACRP.
  • Previous work in research study coordination or experience working in an IRB or experience with working in CRBB.
  • Ability to adapt quickly to changes in work requirements and assignments; must exhibit diplomacy and compassion.

Compensation, Benefits and Position Details

Pay Range Minimum:

$66,000.00 annual

Pay Range Maximum:

$78,000.00 annual

Other Compensation:

-

Benefits:

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 – on our campuses, in our state and around the world.

UW employees bring their boundless energy, creative problem-solving skills and dedication to building stronger minds and a healthier world. In return, they enjoy outstanding benefits, opportunities for professional growth and the chance to work in an environment known for its diversity, intellectual excitement, artistic pursuits and natural beauty.

Our Commitment

The University of Washington is committed to fostering an inclusive, respectful and welcoming community for all. As an equal opportunity employer, the University considers applicants for employment without regard to race, color, creed, religion, national origin, citizenship, sex, pregnancy, age, marital status, sexual orientation, gender identity or expression, genetic information, disability, or veteran status consistent with UW Executive Order No. 81.

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.

Sponsorship evidence

Why Openbound reached the conclusions above.

Visa sponsorship evidence

Current posting

Silent on sponsorship

Other openings

3 of 354 recent openings at this employer mention sponsorship.

Employer H-1B history

195
recent certified H-1B filings
112
new-hire petitions
1
filings for similar roles
153
so far in FY2026

Filed titles like this role: research study coordinator 2

More evidence details
  • 1 certified H-1B filing for this same role
  • 195 recent certified H-1B filings across the employer
  • Still filing this year — 153 filings in FY2026
  • 183 USCIS H-1B new-employment approvals, counted separately from LCA filings
  • Strong filing activity in WA
  • 3 other recent postings at this company mention sponsorship
  • 187 further USCIS approvals for extensions or transfers
  • The posting says nothing about sponsorship either way

Strong filing activity in WA.

Green card sponsorship evidence

Employer PERM history

25
recent certified PERM filings
0
filings for similar roles
25
filings in this location
Certified PERM filings by fiscal year
202314
202429
202527
202624YTD

Filing history reflects past employer behavior; it isn't a promise for this opening.

All open roles at University of Washington
How Openbound evaluates sponsorship

Visa history uses official U.S. Department of Labor H-1B LCA disclosure data and USCIS H-1B petition history. Green card history uses DOL PERM disclosure data. Each is read for the employer as a whole, for roles like this one, and for this location, weighted toward the most recent fiscal years.

An employer is matched to its filing entities by verified legal name and reviewed aliases; a match is never made on a name resemblance alone. Where no verified entity can be matched, the page says so and draws no conclusion from the absence. 45 filing titles were examined for this employer.

What this posting states outranks history in both directions, and an employer's published policy outranks past filings. Filing history reflects past behavior; it is not a promise of sponsorship for this opening, and none of this is legal advice.