About The Position

We are seeking a motivated and detail-oriented Associate Scientist to join our Preclinical Pharmacology team in Lexington, MA. This is a hands-on laboratory role supporting both in vivo and in vitro pharmacology studies, with a primary focus on immunology, inflammation, metabolic disease, fibrosis, and other non-tumor therapeutic areas. The ideal candidate will have strong hands-on experience with mouse studies and preclinical pharmacology, including animal dosing, sample collection, disease model execution, and therapeutic efficacy evaluation. This individual will also support cell-based assays and analytical methods such as ELISA, MSD, and qPCR. This role is well suited for someone who is comfortable working in a fast-paced CRO environment where multiple studies and client projects may be conducted simultaneously.

Requirements

  • Bachelor's or Master’s degree in Pharmacology, Biology, Biochemistry, Toxicology, Immunology, Biomedical Sciences, or a related field.
  • 3+ years of hands-on experience with mouse studies and in vivo experimental procedures.
  • Experience with animal handling, dosing, blood collection, tissue collection, and necropsy.
  • Experience with cell culture and in vitro laboratory techniques.
  • Working knowledge of ELISA, MSD, qPCR, or similar molecular and biochemical assays.
  • Strong attention to detail with the ability to accurately collect, organize, and document experimental data.
  • Ability to work independently while collaborating effectively within a multidisciplinary team.
  • Hands-on, adaptable, and comfortable working on multiple projects in a fast-paced CRO environment.

Nice To Haves

  • Experience establishing or executing mouse disease models strongly preferred.
  • Experience with PK/PD studies and biological sample processing preferred.
  • Experience with metabolic disease models, including obesity, diabetes, NASH/MASH, or related models, is highly desirable.
  • Experience with fibrosis models involving liver, lung, kidney, or other organs is highly desirable.
  • Experience supporting therapeutic efficacy studies for cell therapies, including CAR-T therapies, is a plus.

Responsibilities

  • Execute and support in vivo efficacy studies using non-tumor disease models, including immunology, inflammation, metabolic disease, fibrosis, and autoimmune disease models.
  • Perform routine animal procedures including handling, health monitoring, PO/IP/SC/IV dosing, blood collection, necropsy, and tissue collection.
  • Establish, maintain, and execute mouse disease models to support preclinical drug development programs.
  • Evaluate therapeutic efficacy using appropriate clinical, biochemical, histological, and molecular endpoints.
  • Support study planning, dose formulation, dosing schedules, and biological sample collection strategies.
  • Conduct and support pharmacokinetic (PK) and pharmacodynamic (PD) studies, including biological sample collection and processing.
  • Maintain accurate study records, raw data, sample inventories, and experimental documentation.
  • Identify and communicate unexpected findings, study deviations, or technical issues to the study director.
  • Perform cell-based assays to support drug screening, efficacy evaluation, and mechanism-of-action studies.
  • Culture and maintain mammalian cell lines and primary cells as needed.
  • Conduct laboratory assays including ELISA, MSD, qPCR, cytokine assays, inflammatory biomarker assays, and other biochemical or cellular methods.
  • Process and analyze biological samples collected from in vivo studies.
  • Support assay development, optimization, troubleshooting, and implementation of new methods.
  • Assist with data analysis, interpretation, and preparation of study reports.
  • Work closely with study directors, scientists, and other team members to execute client studies accurately and efficiently.
  • Manage multiple studies and experimental priorities while meeting project timelines.
  • Follow established SOPs, study protocols, animal welfare requirements, and laboratory safety procedures.
  • Contribute to troubleshooting and continuous improvement of experimental methods and study workflows.
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