Principal Investigator ​/ LCMS Scientist

Principal Research Scientist – LC-MS/MS Bioanalysis

Everett, Washington | Relocation Assistance Available

RPM ReSearch has partnered with a leading preclinical Contract Research Organization (CRO) to identify a Principal Research Scientist – LC-MS/MS to join its growing bioanalytical sciences team. Our client partners with pharmaceutical and biotechnology companies to support the discovery and development of novel therapeutics through high-quality GLP bioanalytical services. This is an opportunity to join a collaborative scientific organization where your expertise will directly contribute to advancing new therapies toward the clinic.

Important Qualification

Experience supporting Antibody-Drug Conjugate (ADC) bioanalysis is required for this position.

While we welcome applicants with strong LC-MS/MS backgrounds, this particular opportunity requires prior experience developing, validating, and/or supporting LC-MS/MS methods for ADCs within a GLP pharmaceutical or CRO environment. Candidates without ADC experience are unlikely to be a match for this role.

As the Principal Research Scientist, you will serve as the technical and scientific expert for LC-MS/MS bioanalysis, with particular emphasis on ADCs and large molecule assays. You'll provide scientific leadership across method development, validation, sample analysis, study execution, and client interactions while collaborating closely with cross-functional scientific and regulatory teams in a GLP environment.

• Provide scientific leadership for LC-MS/MS bioanalysis supporting both small and large molecule programs, including ADCs.
• Lead method development, validation, troubleshooting, and sample analysis for GLP bioanalytical studies.
• Serve as Principal Investigator or lead scientist on client-sponsored studies.
• Partner directly with pharmaceutical and biotechnology clients, providing technical expertise and scientific consultation.
• Prepare and review scientific reports, study documentation, and laboratory records.
• Ensure compliance with GLP regulations, FDA guidance, SOPs, and quality standards.
• Collaborate with Quality, Regulatory, and laboratory teams to support successful study execution and continuous process improvement.

The successful candidate will have:

• Bachelor's, Master's, or Ph.D. in Chemistry, Biology, Immunology, or another relevant scientific discipline.
• Significant hands-on experience with LC-MS/MS instrumentation and bioanalytical method development.
• Demonstrated experience supporting Antibody-Drug Conjugate (ADC) bioanalysis.
• Experience working within a GLP-regulated CRO or pharmaceutical environment.
• Experience serving as a Principal Investigator, Senior Research Scientist, or comparable scientific leadership role.
• Strong scientific writing, data interpretation, and client communication skills.
• Ability to manage multiple studies while maintaining exceptional scientific quality and regulatory compliance.

Experience with one or more of the following is highly desirable:

• Large molecule LC-MS/MS assays
• Shimadzu and/or SCIEX instrumentation
• Watson LIMS
• FDA ICH M10 guidance
• Bioanalytical method validation in support of drug development

• Join a respected and growing preclinical CRO supporting innovative pharmaceutical and biotechnology companies.
• Play a highly visible scientific leadership role with direct client interaction.
• Work on cutting-edge therapeutics, including Antibody-Drug Conjugates and other advanced modalities.
• Collaborate with an experienced team of scientists in a GLP environment committed to scientific excellence.
• Competitive compensation, comprehensive benefits, and relocation assistance are available for qualified candidates.