Overview
In this role, you will drive in vivo efficacy and PK/PD studies to evaluate novel cancer therapies. You will build and use CDX, PDX and syngeneic models within a multidisciplinary oncology pharmacology team to support early drug discovery. You will analyze data, communicate findings, and ensure rigorous documentation and adherence to animal protocols. This position offers a meaningful chance to impact preclinical decisions in a leading oncology portfolio.
Pay / Benefits
- performance-based cash incentive
- eligibility for annual equity awards
- comprehensive health, life and disability benefits
- 401(k) with company contribution and match
- generous time off package
- reasonable accommodations
Responsibilities
- Execute pre-clinical in vivo studies to test hypotheses and screen compounds
- Develop and utilize CDX, PDX, and syngeneic tumor models to assess anti-tumor activity, PK/PD, and biomarkers
- Collaborate with pharmacology team to design and run studies independently
- Analyze and present results within a multidisciplinary team
- Maintain strict adherence to animal protocols and document data/methods in electronic notebooks
Key requirements
- BS/MS in biological sciences with 2+ years (Sci I) or 4+ years (Sci II) in pharmaceutical/biotech industry
- Extensive experience with CDX/PDX xenograft and/or syngeneic models
- Experience with cell culture
- Hands-on mouse/rat handling and dosing (IV, IP, PO), tumor implantation, caliper measurements, imaging, and tissue collection
- Experience with PCR, ELISA, western blot, and flow cytometry
- Strong analytical, written and verbal communication skills; proficient in PowerPoint and data analysis tools (Excel, Prism)
- Highly motivated
- Inquisitive and creative
- Thrives in a matrixed, cross-functional environment
- In vivo tumor models: CDX, PDX, syngeneic
- Cell culture
- Mouse/rat handling and dosing (IV, IP, PO)
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