Bioanalyst
- Pay
- $120,200 – $141,960 per year
- Location
- Bothell, WA · On-site
- Job type
- Full-time
- Level
- Mid-level
- Experience
- 5+ years
- Listed
- 30 days ago
Skills & highlights for this role
- bioanalytical assay development
- LC-MS/MS
- ligand-binding assays
- GLP / GCLP / ICH M10
Also useful
- ADC bioanalysis
- CRO management
Position Overview
The Bioanalyst will be responsible for developing and implementing bioanalytical assays to support clinical stage bioanalysis for candidate drugs. In this role, they will participate in the design, development, and implementation of the bioanalytical strategy for multiple oncology programs. This role reports to the Associate Director, Bioanalytical.
Responsibilities
- Develop and implement bioanalytical assays for compounds in clinical development. This includes scientific and technical oversight of CROs performing the bioanalytical lab work as well as ensuring scientific and regulatory compliance.
- Act as the primary contact and maintain working relationships with external vendors to facilitate execution of bioanalytical strategies.
- Actively partner with other functions and departments to ensure that programs are progressed seamlessly through the development process; ensure bioanalytical subject matter expertise is represented in cross-functional project teams.
- Author relevant sections of clinical study protocols, analysis plans, reports and regulatory submissions (such as IBs, CTDs, INDs, BLAs).
Qualifications
- A minimum of 5 years' experience in pharmaceutical/biotechnology industry in a regulated bioanalytical environment, preferably with multiple modalities, including small molecules, large molecules, and ADCs.
- A minimum of 3 years of experience managing relationships with global bioanalytical vendors (CRO's) is required.
- Familiarity with current global bioanalytical regulatory guidance.
- Regulated lab experience (GLP, GCLP, ICH M10).
- History of hands-on bench-level experience with method development, validation, and troubleshooting is required. (Ligand-binding and/or LC-MS/MS).
Knowledge and Skills
- Demonstrated experience supporting clinical and regulatory development of bioanalytical requirements, GxP regulations, with excellent working knowledge of the regulatory process.
- Excellent problem-solving skills and ability and desire to oversee multiple projects simultaneously in a fast-paced environment.
- Demonstrated experience in the development and execution of bioanalytical plans to support clinical development.
- Outstanding interpersonal and communication skills (written and oral) with ability to communicate complex information succinctly.
- Experience authoring relevant sections of global regulatory submissions and interacting with global health authorities.
- Ability to drive collaboration, achieve results, influence, and resolve conflicts across internal and external project teams.
Pay and benefits
Washington State Pay Range $120,200—$141,960 USD
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.
Equal opportunity and legal notices
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).
Immunome, Inc. is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
From Immunome, Inc.'s careers page, first listed on Rolev.ai on October 10, 2026. Rolev.ai is not the employer.
How Rolev.ai helps with this application
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Common questions
What is the salary for the Bioanalyst role at Immunome, Inc.?
The Bioanalyst posting at Immunome, Inc. states compensation of $120,200 – $141,960 per year. It is listed as a full-time position. Final pay may depend on location, experience, and interview evaluation on Immunome, Inc.'s official career site.
Where is the Bioanalyst job at Immunome, Inc. located?
This Bioanalyst position at Immunome, Inc. is located in Bothell, WA (On-site). Always check Immunome, Inc.'s application page for specific state eligibility or relocation policies.
What qualifications are required for Bioanalyst at Immunome, Inc.?
For the Bioanalyst role, Immunome, Inc. highlights 5+ years of relevant experience; experience with bioanalytical assay development, LC-MS/MS, ligand-binding assays, GLP / GCLP / ICH M10. Rolev.ai can score your existing resume against these requirements and show any skill gaps before you apply.
How do I apply for the Bioanalyst position at Immunome, Inc.?
This listing links directly to Immunome, Inc.'s Greenhouse application page. You can apply directly on Immunome, Inc.'s site, or use Rolev.ai to check your resume fit, generate a zero-hallucination tailored resume and cover letter for this posting, and autofill the Greenhouse application form in 1 click with the Rolev.ai Chrome extension. You always review the form and press Submit yourself.