Associate Scientist/Scientist I, In Vivo Pharmacology (Contract)

Mirai Bio, Inc.Cambridge, MA
$46 - $60

About The Position

Mirai is seeking a contract Associate Scientist/Scientist I to join the Translational Biology team and support in vivo laboratory research activities toward the development of novel technologies enabling next-generation genomic medicines. The successful candidate will have a strong understanding of the technical and equipment needs of an in vivo lab, along with significant hands-on experience in rodent in vivo techniques and standard molecular and cell biology assays used to characterize novel formulations. This role requires greater independence than an entry-level associate position: the Scientist I is expected to design experiments, troubleshoot independently, and contribute to the direction of in vivo studies, while working closely and collaboratively with a cross-functional team.

Requirements

  • BS or MS degree in addition to relevant industry experience
  • Associate Scientist: BS and 8+ years or MS degree and 6+ years of industry experience
  • Scientist I: BS and 10+ years or MS degree and 8+ years of industry experience
  • Significant hands-on experience working with small laboratory animals (mice), preferably in a biotech or pharmaceutical environment.
  • Well-established, independent experience with rodent in vivo dosing and handling techniques.
  • Experience in tissue dissection and tissue preparation for histology, RNA, and protein analysis.
  • Experience with molecular and cell biology techniques such as ELISA, FACS/flow cytometry, RT-PCR, and Luminex assays.
  • Working knowledge of analysis tools such as Excel, GraphPad, and PowerPoint for experimental documentation and data analysis/presentation.
  • Demonstrated ability to work independently and collaboratively across highly skilled, cross-functional teams in a fast-paced, entrepreneurial, and technically complex environment.
  • Proficient in primary and cell line culture techniques, with demonstrated ability to execute protocols, troubleshoot assays, and perform literature reviews to evaluate and refine experimental methods.
  • Strong organizational and analytical problem-solving skills, with meticulous attention to detail.
  • Self-motivated, intellectually curious, and comfortable engaging with complex scientific projects and technical teams.

Nice To Haves

  • Hands-on experience with a variety of cell and sample types, including immune cells; expertise in tissue processing and flow cytometry characterization is a plus.
  • Prior experience working with lipid nanoparticles (LNPs) is preferred.

Responsibilities

  • Design and conduct in vivo (mouse) studies to characterize and assess the function, pharmacokinetics, and biodistribution of novel formulations, with increasing ownership of study design and interpretation.
  • Perform hands-on dosing of mice (including intravenous and other routes) and isolation/processing of mouse blood and tissues.
  • Lead or support the development of new in vivo models, including humanized mouse models, live-animal bioluminescent or fluorescence imaging, in vivo target discovery models, and development/optimization of mouse tumor models.
  • Execute and optimize lab procedures such as tissue lysis, ELISA, Western blot, RNA/DNA extraction, qPCR, flow cytometry, and related cell/molecular biology assays supporting in vivo studies.
  • Develop new assays or optimize existing ones based on in-depth knowledge of laboratory techniques, including experimental planning and execution.
  • Analyze, interpret, and accurately document study and assay results in an electronic lab notebook or other technical reporting formats, and present findings in internal meetings.
  • Apply strong experimental design, troubleshooting, and data analysis skills to resolve issues and improve study quality and throughput.
  • Collaborate cross-functionally and may provide guidance or informal mentorship to research associates supporting in vivo work.

Benefits

  • Certain employee benefits may be available to the contractor through the staffing company after meeting minimum criteria.
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