Bioanalyst
Company websiteimmunome.com (Immunome, Inc, opens in new tab)
Base salary $120,200 to $141,960
Employer-published annual base salary, USD. Advertised base range in Bothell, WA
You apply on the employer's own site. Six Figure Work does not handle applications.
- LocationBothell, WA
- WorkplaceWorkplace not stated
- Status at last checkSource accepting applications when checked
- Last checked (3 h ago) · observed since
About this job
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 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.
Washington State Pay Range
$120,200—$141,960 USD
Join Our Experienced, Passionate Team
Working at Immunome gives you the opportunity to make a difference in the lives of cancer patients, contribute to developing best-in-class targeted cancer therapies, and work with some of the brightest and most experienced minds in antibody-drug conjugate (ADC) development.
Immunome’s office is charged with the collective excitement and passion of people working together to develop life-changing cancer medicines. Our team thrives in an innovative, collaborative environment where employees are empowered to do their best work.
Immunome also offers a comprehensive benefit program for you and your family, including:
- Medical, dental, and vision insurance coverage for employees and their dependents, including 100% company-paid medical premiums for employees
- A 401(k) with employer match
- Employer-paid life insurance, short- and long-term disability insurance, and AD&D
- Paid time off, company holidays, and a week-long winter break between Christmas and New Years.
- Paid parental leave
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).
Source: Immunome, Inc on Greenhouse · View original posting (opens in new tab)
This listingBioanalyst$120,200 to $141,960
Senior / Principal Scientist, Formulation and Drug Product Development$155,896 to $190,220
Senior Manager, IT Service Desk$162,000 to $193,562
Principal Scientist, Chemical Development$169,593 to $206,233
Principal Scientist, Analytical Development and QC, Small Molecule$170,000 to $196,227
Associate Director / Director, Supplier Quality and Audits$175,100 to $239,998
Associate Director / Director, Regulatory Affairs CMC$177,399 to $238,957
Chart as a table
| Role | Published base |
|---|---|
| Bioanalyst (this listing) | $120,200 - $141,960 |
| Senior / Principal Scientist, Formulation and Drug Product Development | $155,896 - $190,220 |
| Senior Manager, IT Service Desk | $162,000 - $193,562 |
| Principal Scientist, Chemical Development | $169,593 - $206,233 |
| Principal Scientist, Analytical Development and QC, Small Molecule | $170,000 - $196,227 |
| Associate Director / Director, Supplier Quality and Audits | $175,100 - $239,998 |
| Associate Director / Director, Regulatory Affairs CMC | $177,399 - $238,957 |
Observed changes
- First observed on the employer's board
- Began meeting the published-salary criteria
- Observed since
- Employer-stated posting date
- 2026-09-24
Where this pay comes from
Location as the employer wrote it: Bothell, Washington, United States
$120,200—$141,960 USD
- Method
- Employer text, read with fixed rules and re-verified
- Checked
- Rule set
- us-base-v2
The pay passage appears in the employer's own job text. Fixed, deterministic rules located it, and the passage below was checked against the stored copy of the posting.
What we verified
- The pay figures come from the employer's own listing, quoted exactly above.
- The pay is an annual base salary in US dollars with a minimum of at least $100,000.
- The role was publicly listed on the employer's job board when last checked.
We do not verify what the employer will actually offer, whether the employer is still recruiting for the role, or anything beyond what the employer published. Full methodology.
