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Gene Therapy Jobs in Raleigh, NC (NOW HIRING)

AskBio

Process Engineer II

Durham, NC · On-site

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 ...

AskBio

Process Engineer II

Durham, NC

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 ...

AskBio

Associate Scientist, AS&T

Durham, NC · On-site

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 ...

AskBio

Associate Scientist, AS&T

Durham, NC

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 ...

AskBio

Director, Pathology

Durham, NC · On-site

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 ...

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Showing results 21-40

All JobsGene Therapy JobsGene Therapy Jobs in Raleigh, NC

Gene Therapy information

See Raleigh, NC salary details

$11

$23

$39

How much do gene therapy jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for gene therapy in Raleigh, NC is $23.24, according to ZipRecruiter salary data. Most workers in this role earn between $17.74 and $25.72 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in gene therapy roles?

To thrive in Gene Therapy, you need a strong background in molecular biology, genetics, and biomedical sciences, typically supported by an advanced degree such as a Master's or PhD. Familiarity with laboratory techniques like CRISPR, PCR, viral vector production, and experience using laboratory information management systems (LIMS) are common requirements. Attention to detail, strong problem-solving abilities, and effective teamwork are crucial soft skills in this field. These competencies ensure safe, effective research and development of gene therapies, driving innovation and compliance in a highly regulated environment.

What is gene therapy and how does it work?

Gene therapy is a medical technique that involves introducing, removing, or altering genetic material within a person's cells to treat or prevent disease. This approach aims to correct defective genes responsible for disease development or to provide new genes that help the body fight or prevent a disease. Gene therapy can be delivered using various methods, such as viral vectors or CRISPR-based gene editing. It has shown promise in treating conditions like certain genetic disorders, some types of cancer, and rare inherited diseases. However, gene therapy is still being researched, and its long-term effects and safety are continuously evaluated.

How to get a job in gene therapy?

To work in gene therapy, you need to earn a bachelor’s degree in biology, biochemistry, genetics, or a related field, followed by advanced qualifications, which may include a doctoral degree and demonstrable knowledge of the technologies scientists use to create and use gene therapy vectors and test their efficacy. Coursework in psychology and statistics and experience in a genetic counseling environment can provide further context for your efforts and goals. In many roles, good project management and reporting skills are an asset. Additionally, you should be able to effectively communicate and collaborate with a team of diversely skilled professionals.

What is the difference between Gene Therapy vs Clinical Research Coordinator?

AspectGene TherapyClinical Research Coordinator
Required CredentialsAdvanced degrees in genetics, molecular biology, or related fields; specialized training in gene editing techniquesBachelor's degree in health sciences, biology, or related fields; certification often preferred
Work EnvironmentLaboratories, biotech companies, hospitals conducting gene therapy researchClinical trial sites, hospitals, research institutions overseeing patient studies
Employer & Industry UsageBiotech firms, pharmaceutical companies, academic research centersHospitals, research organizations, pharmaceutical companies

Gene Therapy professionals focus on developing and applying genetic treatments, often working in labs and biotech firms. Clinical Research Coordinators manage patient trials, ensuring protocol adherence in clinical settings. While both roles are vital in medical research, they differ in focus, environment, and required qualifications.

What are some common challenges faced by professionals working in gene therapy research and development?

Professionals in gene therapy often encounter challenges related to the complexity of genetic engineering, ensuring the safety and efficacy of treatments, and navigating strict regulatory requirements. Collaboration across multidisciplinary teams—such as molecular biologists, clinical researchers, and regulatory specialists—is vital for progressing therapies from the lab to clinical trials. Additionally, staying current with rapidly evolving technologies and addressing ethical considerations are important aspects of the role. These challenges make the work both demanding and rewarding, offering significant opportunities for learning and professional growth.

What can you do with gene therapy?

A gene therapy professional develops and applies treatments that modify or replace faulty genes to treat genetic disorders, cancers, and certain viral infections. This role involves working with advanced techniques such as viral vectors, CRISPR, and molecular biology tools in research or clinical settings. Certification and knowledge of genetics, laboratory skills, and regulatory compliance are important for this job.
More about Gene Therapy jobs

What job categories do people searching Gene Therapy jobs in Raleigh, NC look for?

The top searched job categories for Gene Therapy jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Gene Therapy jobs?

Cities near Raleigh, NC with the most Gene Therapy job openings:

Gene Therapy jobs near you
Infographic showing various Gene Therapy job openings in Raleigh, NC as of August 2026, with employment types broken down into 83% Full Time, and 17% Contract. Highlights an 94% In-person, and 6% Remote job distribution, with an average salary of $48,333 per year, or $23.2 per hour.

Associate Scientist, AS&T

Asklepios BioPharmaceutical, Inc.

Durham, NC

Full-time

Posted 18 days ago

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.

Analytical support

  • Lead the development and implementation of phase-appropriate analytical control strategies for gene therapy products, integrating scientific expertise, regulatory expectations, and product knowledge to ensure robust product characterization and lifecycle support.

  • Apply advanced scientific knowledge and broad analytical expertise to direct lifecycle management of complex bioanalytical methods, including but not limited to PCR/ddPCR, ELISA, cell-based potency assays, NGS, HPLC, and AUC, driving method evolution, troubleshooting complex technical challenges, and enabling program objectives.

  • Guide the design and execution of scientifically sound method qualification, validation, transfer, and comparability strategies for rAAV programs, leveraging comprehensive understanding of regulatory requirements, assay performance, and product development considerations.

  • Integrate and interpret analytical data across multiple programs and functional disciplines to identify trends, assess method variability and provide strategic recommendations that support product quality, process understanding, and decision-making.

  • Apply statistical methodologies and scientific judgment to evaluate assay performance, capability, robustness, and lifecycle suitability, developing innovative approaches to address complex analytical challenges and improve data-driven decision-making.

  • Drive continuous improvement and innovation in analytical sciences through the advancement of emerging technologies, digitalization, automation, and novel scientific approaches, guiding the development of new procedures, enhancing operational efficiency, and strengthening analytical capabilities across the organization

Tech transfer and external partner management

  • Lead analytical method transfers across CDMOs, CROs, and internal QC laboratories, applying broad scientific expertise and strategic oversight to ensure successful implementation, knowledge transfer, and sustained method performance throughout the product lifecycle

  • Author, review, and approve transfer protocols, validation strategies, technical reports, and scientific justifications, ensuring alignment with regulatory expectations, quality standards, and program objectives while advancing best practices in analytical sciences

  • Serve as the Analytical Sciences & Technology (AS&T) subject matter expert for external partners, leveraging technical knowledge and cross-functional understanding to establish scientific alignment, resolve complex analytical issues, and drive effective outcomes across organizational boundaries.

  • Lead troubleshooting and resolution of cross-site analytical challenges by integrating scientific principles, data-driven approaches, and multidisciplinary expertise to ensure method consistency, robustness, comparability, and compliance across global laboratory networks.

Quality support

  • Provide scientific oversight for complex analytical investigations, including OOS, OOT, and deviation events, applying technical expertise, data-driven methodologies, and multidisciplinary knowledge to aid in the identification of root causes, assess impact, and develop effective resolution strategies.

  • Partner with Quality, Manufacturing, Regulatory, and other functional areas to develop, and implement, scientifically sound CAPAs, ensuring sustainable improvements, operational excellence, compliance, and alignment with company objectives.

  • Drive inspection readiness by providing scientific leadership in the evaluation, documentation, and resolution of analytical quality events, ensuring robust investigation practices, regulatory compliance, and continuous improvement across the analytical lifecycle.

Regulatory

  • Author and review analytical sections of global regulatory submissions (IND, BLA, MAA), leveraging expertise in analytical control strategies and regulatory requirements to support successful product development and registration

  • Participate in the development and continuous evolution of analytical control strategies, integrating multidisciplinary scientific insights, product knowledge, and emerging regulatory guidance to ensure robust product quality, control, and lifecycle management.

  • Support regulatory interactions, inspections, and responses as an analytical SM

Minimum Requirements

  • Bachelor's degree in biology,microbiology,molecularbiology,biotechnology or related field with 8+ years of relevant work experience, or a Master's degree with 4+ years of relevant work experience

  • Demonstrated experience working in matrix organizations and independent management of cross-functional initiatives

  • Ability to influence without direct authority across teams and functions

  • Hands-on experience supporting GMP environments

  • Experience with method validation, transfer, and lifecycle management

  • Knowledge of analytical methods supporting biologics manufacturing

  • Understanding ICH, FDA, and EMA requirements for gene therapy products.

  • Excellent written and verbal communication skills

  • High attention to detail and data integrity mindset

  • Strong problem-solving and investigative skills

Preferred Education, Experience and Skills

  • Industry experience with strong focus on gene therapies analytical methodologies

  • Experience with stability studies and impurity profiling

  • Project management and prioritization skills

  • Experience supporting regulatory filings and agency interactions

  • Knowledge of Quality by Design (QbD) and risk-based approaches


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 jobrelated 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 careers@askbio.com.

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.

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