Biotech & Pharma OPT Jobs in Washington
Washington state is one of the strongest markets in the U.S. for biotech and pharma F-1 OPT sponsorship jobs, anchored by major employers like Amgen, Seagen (now part of Pfizer), and the University of Washington's life sciences ecosystem. Seattle and the surrounding Puget Sound corridor concentrate the most opportunities, with roles spanning research, clinical development, and bioprocessing.
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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).
OPT Biotech & Pharma Job Roles in Washington
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Search Biotech & Pharma Jobs in WashingtonBiotech & Pharma OPT Sponsorship Jobs in Washington: Frequently Asked Questions
Which biotech & pharma companies sponsor F-1 OPT visas in Washington?
Washington is home to several established biotech and pharma employers with histories of hiring international students on F-1 OPT, including Amgen's Seattle offices, Pfizer (through its Seagen acquisition in Bothell), Adaptive Biotechnologies, and Nuvation Bio. Larger companies with dedicated HR infrastructure tend to have more structured OPT sponsorship processes, though sponsorship is never guaranteed and varies by role and department.
Which cities in Washington have the most biotech & pharma F-1 OPT sponsorship jobs?
Seattle and Bothell account for the largest share of biotech and pharma OPT sponsorship jobs in Washington. Bothell in particular has become a significant life sciences hub, hosting oncology and specialty pharma operations. Redmond and Kirkland also have biotech presence. The University District and South Lake Union neighborhoods in Seattle are especially active, given their proximity to UW research centers and biotech startups.
What types of biotech & pharma roles typically qualify for F-1 OPT sponsorship?
F-1 OPT authorization is tied to your field of study, not the employer's willingness to sponsor. In biotech and pharma, roles that align with STEM degrees commonly include research associate positions, bioprocess engineer roles, computational biology analyst jobs, clinical data management, and regulatory affairs coordinator positions. STEM OPT extension applicants must ensure the role is directly related to their qualifying STEM degree and that the employer participates in E-Verify.
How do I find biotech & pharma F-1 OPT sponsorship jobs in Washington?
Migrate Mate is built specifically for international students and filters biotech and pharma jobs in Washington by visa type, including F-1 OPT sponsorship. Rather than manually screening hundreds of postings, you can search roles already tagged for OPT eligibility across Seattle, Bothell, and other Washington hubs. Migrate Mate also surfaces employers with documented sponsorship histories in the life sciences sector, which saves significant time during an active OPT window.
Are there any Washington-specific considerations for F-1 OPT sponsorship in biotech & pharma?
Washington's biotech sector has a notable concentration of oncology and genomics companies, which tend to require highly specialized graduate-level degrees, so your degree alignment matters more here than in generalist markets. Washington has no state income tax, which affects total compensation comparisons. Additionally, many smaller biotech startups in the state do not participate in E-Verify, which is a firm requirement for STEM OPT extension eligibility, so it is worth confirming E-Verify status before applying.