Research Associate Visa Sponsorship Jobs in Washington
Washington is one of the most active states for research associate visa sponsorship, driven by major employers like the University of Washington, Fred Hutchinson Cancer Center, and Microsoft in the life sciences, biotech, and technology sectors. Seattle and the surrounding Puget Sound region concentrate most opportunities, with additional roles in Spokane and Pullman near Washington State University.
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Get Access To All JobsCompany Overview
Immunome is a clinical-stage targeted oncology company committed to developing first-in-class and best-in-class targeted cancer therapies. We are advancing an innovative portfolio of therapeutics, supported by a leadership team with deep experience in the design, development, and commercialization of cutting-edge therapies, including antibody-drug conjugates. Our pipeline includes varegacestat, an investigational gamma secretase inhibitor for which an NDA has been accepted by the U.S. FDA; IM-1021, a clinical-stage ROR1 ADC; IM-1617, a clinical-stage solid tumor ADC; and IM-3050, a clinical-stage FAP-targeted radioligand therapy. We are also advancing a broad portfolio of early-stage ADCs pursuing undisclosed solid tumor targets.
Position Overview
The Senior In-house Clinical Research Associate (Sr. IHCRA) provides hands-on support for the day-to-day execution of clinical trial activities as assigned by Clinical Project Delivery (CPD) and/or Clinical Site and Trial Operations (CSTO). They operate in compliance with protocols, ICH-GCP, and applicable regulation, and Standard Operating Procedures (SOPs). This role supports functional activities across assigned trials, sites, and vendors throughout the trial lifecycle, under the guidance and oversight of CPD and CSTO to help ensure timely, compliant trial execution. The person in this position may participate in cross-trial process improvement initiatives and may also provide guidance to new or more junior team members.
Responsibilities
Project Delivery and Trial Execution Support:
- Assist with completion of assigned project delivery and clinical trial operational tasks in compliance with ICH-GCP, applicable SOPs, and protocols.
- Help implement various study tracking tools and contribute to the development of study-level documents.
- Maintain study timelines as assigned.
- Assist with data review, protocol deviation review, and the query process as assigned.
- Contribute to the development, maintenance and quality control of trial documentation, including study manuals, plans, protocols, instructions, trackers, worksheets, and presentations.
- Help ensure completeness, maintenance, and quality of the Trial Master File.
Site Management and Monitoring Support:
- Support site management and monitoring activities as assigned, including tasks related to site selection and activation, investigational product (IP) and clinical supplies management, site monitoring visit preparation, site-level Informed Consent review, and site contracts management.
- Help develop, distribute, review, track, and file essential documents and study binder documents, troubleshooting related issues to ensure on time delivery at all stages.
- Maintain site- and participant-level tracking.
- Support data cleaning activities as assigned.
Vendor Management Support:
- Assist with day-to-vendor management activities including tracking and workflow management of vendor contracts.
- Support change order and change notification tracking, as assigned.
- May serve as day-to-day vendor contact for assigned activities.
- Participate in vendor teleconferences, record meeting minutes, track action items and decisions.
- Assist with invoice review and budget tracking.
Cross-Functional Collaboration:
- Collaborate with the clinical study team members as assigned to support consistency and efficiency of trial execution.
- Develop and maintain positive, effective, and collaborative working relationships with team members and vendors.
- Help onboard and guide new or junior team members.
Qualifications
- Bachelor’s degree with 3 years of clinical project or trial management experience in the biotechnology or pharmaceutical industry, or an equivalent combination of education and experience.
- Demonstrated experience with site management and vendor management activities, including CROs and central labs.
- Demonstrated experience with trial documentation and Trial Master File management.
Knowledge And Skills
- Working knowledge of clinical trial processes, and ICH-GCP.
- Strong organizational skills with the ability to manage multiple competing tasks.
- Ability to effectively work cross-functionally and build relationships with stakeholders without direct authority.
- Strong communication and interpersonal skills.
- Detail-oriented with an analytical approach to problem-solving.
- Able to prioritize and manage multiple tasks and projects in a fast-paced, dynamic environment.
- Highly professional, adaptable, and accountable.
Washington State Pay Range
$127,890 - $155,682 USD
E/E/O
Immunome, Inc. is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
E-Verify
Immunome, Inc. is a participant in E-Verify. Please review the following notices: E-Verify Participation Poster | Right to Work Poster (English) | Right to Work Poster (Spanish).
Company Overview
Immunome is a clinical-stage targeted oncology company committed to developing first-in-class and best-in-class targeted cancer therapies. We are advancing an innovative portfolio of therapeutics, supported by a leadership team with deep experience in the design, development, and commercialization of cutting-edge therapies, including antibody-drug conjugates. Our pipeline includes varegacestat, an investigational gamma secretase inhibitor for which an NDA has been accepted by the U.S. FDA; IM-1021, a clinical-stage ROR1 ADC; IM-1617, a clinical-stage solid tumor ADC; and IM-3050, a clinical-stage FAP-targeted radioligand therapy. We are also advancing a broad portfolio of early-stage ADCs pursuing undisclosed solid tumor targets.
Position Overview
The Senior In-house Clinical Research Associate (Sr. IHCRA) provides hands-on support for the day-to-day execution of clinical trial activities as assigned by Clinical Project Delivery (CPD) and/or Clinical Site and Trial Operations (CSTO). They operate in compliance with protocols, ICH-GCP, and applicable regulation, and Standard Operating Procedures (SOPs). This role supports functional activities across assigned trials, sites, and vendors throughout the trial lifecycle, under the guidance and oversight of CPD and CSTO to help ensure timely, compliant trial execution. The person in this position may participate in cross-trial process improvement initiatives and may also provide guidance to new or more junior team members.
Responsibilities
Project Delivery and Trial Execution Support:
- Assist with completion of assigned project delivery and clinical trial operational tasks in compliance with ICH-GCP, applicable SOPs, and protocols.
- Help implement various study tracking tools and contribute to the development of study-level documents.
- Maintain study timelines as assigned.
- Assist with data review, protocol deviation review, and the query process as assigned.
- Contribute to the development, maintenance and quality control of trial documentation, including study manuals, plans, protocols, instructions, trackers, worksheets, and presentations.
- Help ensure completeness, maintenance, and quality of the Trial Master File.
Site Management and Monitoring Support:
- Support site management and monitoring activities as assigned, including tasks related to site selection and activation, investigational product (IP) and clinical supplies management, site monitoring visit preparation, site-level Informed Consent review, and site contracts management.
- Help develop, distribute, review, track, and file essential documents and study binder documents, troubleshooting related issues to ensure on time delivery at all stages.
- Maintain site- and participant-level tracking.
- Support data cleaning activities as assigned.
Vendor Management Support:
- Assist with day-to-vendor management activities including tracking and workflow management of vendor contracts.
- Support change order and change notification tracking, as assigned.
- May serve as day-to-day vendor contact for assigned activities.
- Participate in vendor teleconferences, record meeting minutes, track action items and decisions.
- Assist with invoice review and budget tracking.
Cross-Functional Collaboration:
- Collaborate with the clinical study team members as assigned to support consistency and efficiency of trial execution.
- Develop and maintain positive, effective, and collaborative working relationships with team members and vendors.
- Help onboard and guide new or junior team members.
Qualifications
- Bachelor’s degree with 3 years of clinical project or trial management experience in the biotechnology or pharmaceutical industry, or an equivalent combination of education and experience.
- Demonstrated experience with site management and vendor management activities, including CROs and central labs.
- Demonstrated experience with trial documentation and Trial Master File management.
Knowledge And Skills
- Working knowledge of clinical trial processes, and ICH-GCP.
- Strong organizational skills with the ability to manage multiple competing tasks.
- Ability to effectively work cross-functionally and build relationships with stakeholders without direct authority.
- Strong communication and interpersonal skills.
- Detail-oriented with an analytical approach to problem-solving.
- Able to prioritize and manage multiple tasks and projects in a fast-paced, dynamic environment.
- Highly professional, adaptable, and accountable.
Washington State Pay Range
$127,890 - $155,682 USD
E/E/O
Immunome, Inc. is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
E-Verify
Immunome, Inc. is a participant in E-Verify. Please review the following notices: E-Verify Participation Poster | Right to Work Poster (English) | Right to Work Poster (Spanish).
Research Associate Job Roles in Washington
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Search Research Associate Jobs in WashingtonResearch Associate Jobs in Washington: Frequently Asked Questions
Which companies sponsor visas for research associates in Washington?
Major sponsors of research associate roles in Washington include the University of Washington, Fred Hutchinson Cancer Center, Seattle Children's Research Institute, Allen Institute, and Washington State University. Biotechnology firms like Juno Therapeutics and Adaptive Biotechnologies, along with large technology companies in the Seattle area, also regularly file sponsorship petitions for research positions requiring specialized graduate-level training.
Which visa types are most common for research associate roles in Washington?
The H-1B visa is the most common visa for research associates in Washington, applying to roles requiring a bachelor's degree or higher in a directly related field such as biology, chemistry, or data science. University-affiliated positions often use J-1 visa exchange visitor visas for postdoctoral or collaborative research appointments. Some roles at nonprofit research institutions may qualify for cap-exempt H-1B filings, bypassing the annual lottery.
Which cities in Washington have the most research associate sponsorship jobs?
Seattle accounts for the largest share of research associate sponsorship activity in Washington, anchored by its concentration of academic medical centers, biotech firms, and technology companies. Bellevue and Redmond add additional opportunities through corporate research functions. Spokane hosts research positions tied to Washington State University's health sciences programs, and Pullman generates openings through WSU's agricultural and scientific research departments.
How to find research associate visa sponsorship jobs in Washington?
Migrate Mate filters job listings specifically by visa sponsorship availability, making it straightforward to identify research associate roles in Washington where employers have confirmed willingness to sponsor. You can narrow results by city, research field, or institution type. Given the concentration of academic and biotech employers in the Seattle area, filtering for those sectors on Migrate Mate surfaces the most active sponsorship opportunities for research associates in the state.
Are there state-specific considerations for research associates seeking sponsorship in Washington?
Washington's strong university and biotech pipeline means many research associate positions are affiliated with nonprofit or higher-education institutions, which can qualify for cap-exempt H-1B sponsorship outside the annual lottery. The state has no personal income tax, which factors into how employers structure compensation benchmarks for prevailing wage compliance. Research associates in life sciences should also be aware that clinical or laboratory roles may have credential verification requirements beyond the standard visa documentation.
What is the prevailing wage for sponsored research associate jobs in Washington?
U.S. employers sponsoring a visa must pay at least the prevailing wage, which is what workers in the same role, area, and experience level typically earn. The Department of Labor sets this rate to make sure companies aren't hiring foreign workers simply because they'd accept lower pay than a U.S. worker. It varies by job title, location, and experience. You can look up current prevailing wage rates for any occupation and location using the OFLC Wage Search page.