Research Associate
US$106,000 – US$126,000 / yr base salary
Posted 24 Sep 2026
Advertised as “Senior Research Associate, DMPK”
BranchFactor Summary
The original posting with the fluff stripped out
- Expected experience
- 3+ yrs
- Management level
- Individual contributor
- Employment
- On-Site
| Base salary | US$106,000 – US$126,000 / yr |
|---|
Field of studyPharmaceutical Sciences (or related)
Study levelBachelor's or higher
Revolution Medicines is a global, commercial-state oncology company dedicated to discovering, developing and delivering innovative medicines for patients with RAS-addicted cancers. Leveraging its differentiated RAS(ON) tri-complex inhibitor platform, the company is advancing a broad, integrated portfolio of oral RAS(ON) inhibitors designed to directly target the active, cancer-driving state of RAS. Founded on rigorous scientific inquiry and a willingness to challenge long-held assumptions, Revolution Medicines is committed to changing the trajectory of disease for patients with RAS-addicted cancers worldwide.
Our people are united by a shared way of working: follow the science, challenge assumptions, act with urgency and hold ourselves to a high standard of rigor—all in service of patients.
The Opportunity:
As a key member of our dynamic DMPK lab team within DMPK under the non-clinical development and clinical pharmacology (NDCP) department, you will have responsibilities including, but not limited to:
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Develop LC-MS/MS methods and analyze in vivo and in vitro samples to support ADME, pharmacokinetic, efficacy, and toxicokinetic studies, etc.
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Handle a variety of tissues, including tumors, from tissue homogenization through sample preparation for bioanalysis.
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Perform data analysis, prepare experimental result reports, and upload data to electronic notebooks.
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Conduct in vitro ADME/DMPK assays in biological matrices, including hepatocytes, microsomes, blood, and plasma, ect.
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Support laboratory operations, including lab safety, LC-MS/MS instrument maintenance and troubleshooting.
Required Skills, Experience and Education:
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Bachelor’s or master’s degree in pharmaceutical sciences or a related scientific discipline, with 5+ years of industry experience for bachelor’s degree holders or 3+ years for master’s degree holders.
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Hands-on experience in operating and maintaining LC-MS/MS systems.
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Hands-on experience in LC-MS/MS method development and bioanalytical analysis.
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Knowledge of biological sample preparation and extraction techniques for downstream LC-MS/MS analysis.
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Hands-on experience in HPLC/UPLC method development.
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Ability to customize and follow established assay protocols.
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Ability to manage multiple laboratory and project tasks efficiently.
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Ability to work effectively in a flexible, team-oriented environment.