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About the Role
This Research Associate (RA) will support the Analytical Development team by performing routine testing of samples and preparing analytical assays for AAV-based gene therapy programs. Responsibilities include assisting with cell culture maintenance, executing molecular assays like qPCR/ddPCR, and maintaining laboratory organization. The role also involves supporting daily lab operations and requires strong communication, multitasking abilities, and adaptability in a fast-paced setting.
Responsibilities
- Understands and interprets research protocols and procedures.
- Communicates questions, observations, and/or data findings with scientists to resolve challenges and gain scientific understanding.
- Independently performs routine testing methodologies for AAV gene therapy vectors – including assays PCR-based assays and/or ELISA.
- Identifies risks in assay performance, communicates them effectively, and supports mitigation efforts.
- Maintains cell cultures and ensures reagents/supplies are ready-to-use.
- Collaborates across teams to raise awareness and/or to collect, analyze, document and report data.
- Performs routine laboratory activities such as material procurement, media and reagent preparation, and inventory organization.
- Participates in regular team meetings (both in-person and virtually).
Requirements
- BS in Chemistry, Biochemistry, Life Sciences, Pharmaceutical Sciences, Chemical Engineering, or a related field.
- 1 – 3 years of relevant, hands-on experience in academia and/or industry.
- Hands-on experience with gene therapy products is highly desirable.
- Working knowledge of analytical assay development, including molecular, immuno-, and cell-based assays (e.g., dPCR/ddPCR/qPCR, ELISA).
- Basic understanding of FDA regulations, cGxPs, and ICH guidelines is a plus.
- Proficiency in using electronic laboratory notebooks (e.g., Benchling) for documentation, data analysis, and collaboration.
- Strong organizational and problem-solving skills, with the ability to manage multiple tasks in a fast-paced environment.
- A proactive, team-oriented attitude and excellent communication skills.
Skills
- Analytical assay development
- Molecular assays
- Immuno-assays
- Cell-based assays
- dPCR/ddPCR/qPCR
- ELISA
- Electronic laboratory notebooks (e.g., Benchling)
- Documentation
- Data analysis
- Collaboration
- Organizational skills
- Problem-solving skills
- Communication skills
Location
- New York City
Work Type
- Onsite
Experience Level
- 1-3 years
Education Level
- BS
About the Company
- Lexeo Therapeutics is a clinical-stage genetic medicine company headquartered in New York City, pioneering cardiac genetic medicine candidates to treat the root causes of inherited cardiovascular diseases.
- Our lead program, LX2006, targets cardiomyopathy associated with Friedreich’s Ataxia and anchors a broader pipeline addressing genetically defined conditions such as hypertrophic and arrhythmogenic cardiomyopathies.
- Backed by a strong financial foundation, Lexeo is positioned to translate groundbreaking science into durable clinical impact.
Equal Opportunity
- Lexeo Therapeutics is an EEO employer committed to an exciting, diverse, and enriching work environment.