Associate Scientist, Immunology

NCBiotech; Durham (NC); On-site; USD 85,000 - 120,000; Full time

Job summary

AskBio Inc., a gene therapy company, seeks an Associate Scientist to join the Bioanalytical Group in RTP, NC. The role focuses on developing and validating binding and neutralizing antibody assays for preclinical and clinical samples, with hands-on immune assay experience and knowledge of regulatory standards.

Collaboration with cross-functional teams is essential to advance gene therapy programs. The successful candidate will contribute to regulatory submissions, stay current with instrument

Qualifications

• Bachelor’s degree with 8+ years’ relevant work experience, or Master’s with 4+ years’ relevant work experience.
• Experience in Pharma or CRO industry.
• Development and validation of ligand binding and neutralizing antibody assays
• Experience with mammalian cell culture and analytical assays using MSD platform
• Knowledge of FDA guidelines and GLP/CLIA/GCLP compliance

Responsibilities

• Independently design and execute complex antibody assays.
• Optimize and troubleshoot assay protocols for accuracy and reproducibility.
• Perform clinical sample analysis and prepare reports for clinical sites.
• Conduct data analysis using statistical/bioinformatics tools and interpret results.
• Prepare reports, presentations and manuscripts for stakeholders.
• Stay current with advances in gene therapy and apply knowledge to work.
• Collaborate with researchers and engineers to achieve goals.
• Develop and implement SOPs for research quality.

Skills

Communication skills

Team collaboration

Independent work

Organization

Education

Bachelor’s degree in Immunology/Biology/Biochemistry/Biotechnology/Virology

Master’s degree in Immunology/Biology/Biochemistry/Biotechnology/Virology

Tools

MS Office

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

Seeking a highly motivated and detail-oriented Associate Scientist to join our Bioanalytical Group.

The successful candidate will play a key role in developing and validating binding antibody and neutralizing antibody assays performed on preclinical and clinical samples to support our gene therapy programs. This position requires hands‑on experience in immune assay techniques and a basic understanding of gene therapy research. The successful candidate will work closely with cross‑functional teams to ensure that assays meet regulatory standards and contribute to the advancement of gene therapy projects. The ideal candidate will have a strong background in binding antibody assays, cell culture, and aseptic techniques. This position offers an opportunity to work in a dynamic, fast‑paced environment and contribute to the development of innovative gene therapies for patients in need. Antibody assay development, qualification and validation activities will be performed in compliance with GCLP (Good Clinical Laboratory Practices) laboratories, GLP (Good Laboratory Practices), CLIA (Clinical Laboratory Improvement Act), and national, international, and state regulations.

This position is on site in RTP, NC and reports to an Associate Director, Clinical Immunology.

Job Responsibilities

• Independently design and execute complex assays related to neutralizing and total antibody development, utilizing strong scientific expertise and knowledge of adeno viral vector and cell‑based techniques
• Optimize and troubleshoot experimental protocols to ensure accuracy, reproducibility, and efficiency. Perform neutralizing and total antibody assay validation to meet FDA and CLIA guidelines
• Perform clinical sample analysis and prepare comprehensive reports for clinical sites
• Perform in-depth data analysis using advanced statistical and bioinformatics tools, and draw meaningful conclusions from the results
• Prepare comprehensive reports, presentations, and manuscripts summarizing research findings for internal and external stakeholders
• Stay current with the latest advancements in gene therapy research and apply this knowledge to your work
• Collaborate effectively with research scientists, engineers, and other team members to achieve project goals
• Develop and implement standard operating procedures (SOPs) for maintaining consistent research quality
• Assist with the preparation and submission of regulatory filings
• May supervise and mentor junior research staff

Minimum Requirements

• Bachelor’s degree in Immunology, Biology, Biochemistry, Biotechnology, Virology or related field with 8+ years’ relevant work experience; or Master’s degree in Immunology, Biology, Biochemistry, Biotechnology, Virology or related field with 4+ years’ relevant work experience
• Prior experience in Pharma or CRO industry
• Basic lab skills, such as adhering GCLP, biosafety and chemical use guidelines (training provided) and making reagents at desired dilutions or concentrations
• Demonstrated experience in the performing development and validation of ligand binding and neutralizing antibody assay following GLP compliance
• Experience with mammalian cell culture and performing analytical assays using MSD platform
• Knowledge of industry practices for the development, qualification/ validation of immunogenicity assays and FDA guidelines
• Knowledge of Companion Diagnostics
• Proficiency with MS Office tools (Word, Excel, and PowerPoint)
• Self‑motivated, organized, and individual capable of working independently as well as an active team contributor
• Strong oral and written communication skills
• Excellent interpersonal skills with the ability to interact effectively with teams, internally and externally

Preferred Education, Experience and Skills

• Experience in performing Western blots and protein purification. and processing/handling primary cells such as PBMCs

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 [phone] or sending us an email at [e-mail].

Agencies: Please do not contact any employee at AskBio about this requisition. Any resume submitted by a recruitment agency to any employee at AskBio, through any medium, will be deemed the sole property of AskBio unless the agency was engaged by AskBio Talent Acquisition team to recruit for that position. All agencies must have a prior executed service agreement with AskBio prior to any search engagement. If a candidate who was submitted outside of the AskBio agency process is hired by AskBio, no fee or payment of any kind will be paid to the agency.