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Scientist I/II, In Vivo Pharmacology

Read straight from Lexeo TX's careers page, verified 1d ago.Seekless can tailor your résumé to it.
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Before you apply
SalaryNo pay range posted
LocationNew York, New York
Work modeon-site
Typefull-time
SeniorityEntry
ExperienceUp to 3 yrs
DepartmentPre-clinical
Company size51–200 people
PostedOct 21, 2026 · 2w ago
Verified live1d ago
New York law requires most employers to post a pay range.
At a glanceSummarised by Seekless from the posting.
PhD in physiology, pharmacology, cardiovascular biology, or a related field with 0–3 years of postdoctoral or industry experience; or MS with 5+ years of industry experience
Hands-on rodent experience: handling, multi-route dosing, blood collection, survival surgery, and necropsy
Track record using rodent disease models for target validation or efficacy testing of molecules
Proven understanding of power analyses, methods of randomizing animal models and appropriate uses of statistical methods
Strong data analysis skills (e.g., GraphPad) and clear written and verbal communication
Organized and independent; able to run several longitudinal studies at once within a collaborative team
Industry experience in a small, fast-paced biotech is highly preferred
Working knowledge of qPCR/ddPCR for vector/mRNA, ELISA/LC-MS for ASO, RNAscope/IHC for tissue localization, WB/ ELISA/MSD for protein detection
Hands-on echocardiography in mice and rats (e.g., Vevo)
ECG and blood pressure telemetry implantation and analysis in mice and rats (e.g., Ponemah)
Cardiac surgical models (TAC, MI) and invasive hemodynamics (PV-loop)
Demonstrated experience with models of neurodegenerative disease, particularly ataxia or cerebellar disorders, including execution and interpretation of rotarod, gait analysis, balance beam, grip strength, and longitudinal behavioral studies
In vivo experience working with and advancing AAV or oligonucleotide therapeutics
Experience selecting and evaluating CROs to perform animal studies
AALAS certification or equivalent
Ability to regularly work onsite at HQ in New York City
Skills
GraphPad
qPCR
ddPCR
ELISA
LC-MS
RNAscope
IHC
WB
MSD
About the role
Role Summary
Lexeo is seeking a hands-on in vivo pharmacologist to build rodent models of cardiac disease and use them to de-risk targets, screen therapeutic candidates and advance our discovery pipeline. The scientist will design, perform or manage rodent studies from target validation through hit identification, working cross-functionally with In Vitro Pharmacology, Modality Engineering, and Translational Sciences to select-advance molecules. Reporting to the Head of Cardiac Research, this role joins cardiac, neuroscience, and non-clinical scientists developing therapies for genetic heart disease and offers broad experience in multidisciplinary biopharma research.
Primary Responsibilities
•
Design and execute in vivo studies that de-risk novel targets, using genetic knockdown/overexpression and tool molecules to test target–phenotype links
•
Outsource or internally establish rodent cardiac disease models, including transgenic lines and surgical models such as TAC and MI
•
Run therapeutic screening studies that rank candidates on efficacy, dose-response, durability, and identify hit molecules for advancement
•
Dose by multiple routes (IV, IP, SC, IM, PO, retro-orbital) and by osmotic minipump across longitudinal studies
•
Lead study takedowns: necropsy, blood and tissue collection, and processing for histology, molecular, and ex vivo endpoints, including Langendorff cardiac dissociation
•
Partner with Translational Sciences to establish bioanalytical methods for biodistribution and target engagement in rodent tissues, and align on models with clinical endpoints/biomarkers
•
Analyze, interpret, and present data to project teams; keep study records in the ELN in line with IACUC and animal welfare standards
•
Manage study logistics, manage budgets, flag capacity or timeline risks early, and ideate novel methods for pharmacology and physiology
Required Skills and Qualifications
•
PhD in physiology, pharmacology, cardiovascular biology, or a related field with 0–3 years of postdoctoral or industry experience; or MS with 5+ years of industry experience
•
Hands-on rodent experience: handling, multi-route dosing, blood collection, survival surgery, and necropsy
•
Track record using rodent disease models for target validation or efficacy testing of molecules
•
Proven understanding of power analyses, methods of randomizing animal models and appropriate uses of statistical methods
•
Strong data analysis skills (e.g., GraphPad) and clear written and verbal communication
•
Organized and independent; able to run several longitudinal studies at once within a collaborative team
•
Ability to regularly work onsite at HQ in New York City
Preferred Skills and Qualifications
•
Industry experience in a small, fast-paced biotech is highly preferred
•
Working knowledge of qPCR/ddPCR for vector/mRNA, ELISA/LC-MS for ASO, RNAscope/IHC for tissue localization, WB/ ELISA/MSD for protein detection
•
Hands-on echocardiography in mice and rats (e.g., Vevo)
•
ECG and blood pressure telemetry implantation and analysis in mice and rats (e.g., Ponemah)
•
Cardiac surgical models (TAC, MI) and invasive hemodynamics (PV-loop)
•
Demonstrated experience with models of neurodegenerative disease, particularly ataxia or cerebellar disorders, including execution and interpretation of rotarod, gait analysis, balance beam, grip strength, and longitudinal behavioral studies
•
In vivo experience working with and advancing AAV or oligonucleotide therapeutics
•
Experience selecting and evaluating CROs to perform animal studies
•
AALAS certification or equivalent
About LEXEO
Lexeo Therapeutics is a New York City-based, clinical stage company dedicated to reshaping the path of genetic disease. By advancing pioneering science, Lexeo seeks to set a new standard in the treatment of cardiovascular and neurological genetic diseases, charting the path to patient outcomes once thought out of reach. The Company is advancing a portfolio of therapeutic candidates designed to address the underlying genetic causes of disease, including LX2006 for Friedreich ataxia (FA), LX2020 for plakophilin-2 (PKP2) arrhythmogenic cardiomyopathy, and others in devastating diseases with high unmet need.
LEXEO Therapeutics is an EEO employer committed to an exciting, diverse, and enriching work environment.