Senior Research Associate, Biodistribution

askbio; Durham (NC); On-site; USD 85,000 - 125,000; Full time

Job summary

AskBio Inc., a Bayer subsidiary, seeks a Senior Research Associate, Molecular Biodistribution, to execute biodistribution and gene expression experiments at the RTP, NC site. You will perform fit-for-purpose molecular assays, generate tissue distribution and transgene data, and help inform candidate selection, dose strategy, and safety assessments.

The role collaborates with Product Development, Translation Medicine, Tech Ops, and R&D, combining hands-on assay development with data analysis and

Qualifications

• Bachelor's or Master's in molecular biology or related with related work experience (5+ yrs for Bachelor's, 2+ yrs for Master's).
• Experience in biotech/pharma CRO or academic translational research supporting genetic medicine or related modalities.
• Direct experience executing biodistribution and gene expression studies for gene therapy, especially AAV-based programs.
• Hands-on experience with nucleic acid extraction from tissues and biofluids and with qPCR/ddPCR/RT-qPCR.
• Experience supporting preclinical drug development, including non-GLP and/or GLP studies, and regulated documentation.
• Understanding nonclinical development considerations for genetic medicines, including tissue tropism and vector persistence.

Responsibilities

• Develop, optimize, and troubleshoot molecular assays to quantify vector genomes, transgene expression, and related biomarkers in tissues and biofluids.
• Apply and oversee qPCR-based and related molecular methods (ddPCR, RT-qPCR) with proper controls and data quality practices.
• Collaborate with internal stakeholders and external partners for assay transfer and sample analysis.
• Drive continuous improvement in assay sensitivity, specificity, reproducibility, and scalability.
• Analyze biodistribution and gene expression data to inform program decisions and regulatory submissions.

Skills

Molecular biology

Biodistribution

Gene expression analysis

Data interpretation

Cross-functional collaboration

Regulated documentation

Education

Bachelor's degree in molecular biology or related

Master's degree in molecular biology or related

Tools

ddPCR

qPCR

RT-qPCR

Nucleic acid extraction

Job description

AskBio Inc., a wholly owned and independently operated subsidiary of Bayer AG, is a fully integrated gene therapy company dedicated to developing life-saving medicines and changing lives. The company maintains a portfolio of clinical programs across a range of neuromuscular, central nervous system, cardiovascular, and metabolic disease indications with a clinical-stage pipeline that includes investigational therapeutics for congestive heart failure, limb‑girdle muscular dystrophy, multiple system atrophy, Parkinson’s disease, and Pompe disease. AskBio’s gene therapy platform includes Pro10™, an industry‑leading proprietary cell line manufacturing process, and an extensive array of capsids and promoters. With global headquarters in Research Triangle Park, North Carolina, and European headquarters in Edinburgh, Scotland, the company has generated hundreds of proprietary capsids and promoters, several of which have entered pre‑clinical and clinical testing.

Our vision: Pioneering science to create transformative molecular medicines.

Our mission: Lead innovative science and drive clinical outcomes to transform people's lives.

Our principles:

• Advance innovative science by pushing boundaries.
• Bring transformative therapeutics to patients in need.
• Provide an environment for employees to reach their fullest potential.

Our values:

• Be a Pioneer. We are not afraid of the impossible and to innovate to make gene therapies accessible to those in need.
• Cultivate Collaboration. Strive to be the best teammate, actively listen, openly communicate, and embrace diverse points of view.
• Embrace Responsibility. We are humbled by the enormity of our mission.We hold a relentless commitment to advance science and clinical outcomes for our patients, families, and caregivers.
• Raise the Bar. Continuously drive improvements and efficiencies. Seek and provide constructive feedback. Have a bias for learning and action.
• Act with Uncompromising Integrity. Be honest, transparent, and committed to doing what’s right in every situation. Make clear commitments and follow through.

Position Summary

The Senior Research Associate, Molecular Biodistribution executes biodistribution and gene expression assessment experiments. This role is responsible for executing fit-for-purpose molecular assays, generating high‑quality tissue distribution and transgene expression data, and interpreting results to inform candidate selection, dose strategy, safety assessment, and support regulatory submissions.

The role partners closely with Product Development, Translation Medicine, Tech Ops, and Research and Development among other functions. The successful candidate combines hands‑on technical experience with scientific judgment in assay development, data analysis and interpretation, and cross‑functional communication.

This position will be onsite in RTP, NC and will report to the Director, Product Development Cores.

Job Responsibilities

Assay Development and Execution

• Develop, optimize, and troubleshoot molecular assays to quantify vector genomes, transgene expression, and related biomarkers in tissues and biofluids.
• Apply and oversee quantitative PCR‑based and related molecular methods, including qPCR, ddPCR, RT-qPCR, and other nucleic acid quantification approaches.
• Establish assay controls, standards, acceptance criteria, normalization strategies, and data quality practices appropriate for regulated and non‑regulated studies.
• Collaborate with internal stakeholders external partners to ensure reliable assay execution, method transfer, and sample analysis.
• Drive continuous improvement in assay sensitivity, specificity, reproducibility, and operational scalability.

Data Analysis and Interpretation

• Analyze and interpret biodistribution and gene expression datasets to support program decisions in research and development.
• Assess vector genome copy number, transgene RNA expression, and relationships across dose, tissue, timepoint, and platform.
• Identify technical or biological sources of variability and recommend follow‑up experiments or analytical refinements.
• Summarize findings in clear scientific narratives for study reports, governance discussions, and regulatory documentation.
• Present results and recommendations to cross‑functional teams and senior stakeholders.

Minimum Requirements

• Bachelor’s degree in molecular biology, pharmacology, bioanalytical sciences, genetics, biomedical sciences, or a related discipline with 5+ years’ related work experience; OR Master’s degree in molecular biology, pharmacology, bioanalytical sciences, genetics, biomedical sciences, or a related discipline with 2+ years’ related work experience
• Experience in biotech, pharma, CRO, or academic translational research settings supporting genetic medicine or related modalities
• Direct experience executing and interpreting biodistribution and gene expression studies for gene therapy, especially AAV‑based programs
• Hands‑on experience with nucleic acid extraction from tissues and biofluids and with quantitative molecular assay platforms such as ddPCR, qPCR, and RT‑qPCR
• Experience supporting preclinical drug development, including non‑GLP and/or GLP studies, assay qualification, and regulated documentation
• Demonstrated understanding of nonclinical development considerations for genetic medicines, including tissue tropism, vector persistence, transgene expression, and safety assessment

Preferred Education, Experience and Skills

• Experience with AAV gene therapy development across multiple serotypes, capsids, promoters, or routes of administration
• Experience writing data reports and communicating findings and conclusions to scientific personnel
• Knowledge of statistical and data visualization approaches used for complex multidimensional nonclinical datasets

AskBio Inc. (AskBio) is an Equal Opportunity Employer and does not discriminate against any employee or applicant for employment because of race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status or any other protected status prohibited under Federal, State or local laws. All employment decisions are based on valid job‑related requirements. If you are a qualified individual with a disability or a disabled veteran and are unable or limited in your ability to use or access our website, you may request a reasonable accommodation to express interest in a specific opening by calling us at (919) 561‑6210 or sending us an email at [e-mail].