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Gene Therapy Jobs in Raleigh, NC (NOW HIRING)

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 ...

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 ...

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 ...

Manufacturing Associate II

Durham, NC · On-site

$80K - $115K/yr

The ideal candidates will have experience in cell or gene therapy, along with demonstrated ability in a GMP environment. They will also possess the ability to successfully interface with ...

Showing results 41-60

Gene Therapy information

See Raleigh, NC salary details

$11

$23

$39

How much do gene therapy jobs pay per hour?

As of Aug 16, 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.

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:

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.

Director, Pathology

AskBio

Durham, NC • On-site

Other

Re-posted 21 days ago


Job description

Opportunity for Secondment to AskBio

We're pleased to share an exciting secondment opportunity at AskBio.

This role is available for a time period to be determined by leadership at both Bayer and AskBio. While most assignments range from one to two years, the exact duration will be based on business needs and mutual agreement.

This secondment offers a unique chance to broaden your experience, expand your knowledge, and contribute meaningfully to AskBio's mission: to advance gene therapy and change the lives of patients around the world.

If you're interested in exploring this opportunity, we encourage you to:

  • Speak with your direct manager to discuss your interest and alignment with your development goals.
  • Apply directly using the link provided in the posting.

We look forward to seeing how our colleagues continue to grow and make an impact across the Bayer-AskBio partnership.

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 Director Pathology serves as the lead for Translational Medicine Safety (anatomic and clinical pathology & toxicology) of multiple drug candidates of AskBio's pipeline and reports to the Sr. Director, Pathology.

Job Responsibilities
  • Serve as the lead for Translational Medicine (anatomic and clinical pathology & toxicology), shaping the strategy and execution of nonclinical safety assessments
  • Provide comprehensive support for nonclinical studies, including but not limited to pathology peer reviews, interpretation of all nonclinical study data/findings, and guiding study designs, execution, and reporting to support regulatory submissions
  • Act as the Principal Investigator for pathology components of non-GLP and GLP-compliant studies and communicate effectively with CRO pathologists to discuss findings, address questions, and reach the pathology conclusions to ensure high-quality toxicology and pathology assessments
  • Manage and provide scientific leadership to the internal staff and work closely with Discovery, Product Development, Clinical Development, and Regulatory to integrate nonclinical safety findings into overall program strategy and goals
  • Advise and direct the preparation of Toxicology sections of regulatory documents (IND, CTA, NDA, briefing books, Investigator Brochures, etc.)
  • Represent Translational Medicine on discovery and development-IPT and EPT program teams
  • Oversees and drives the preparation of SOPs as needed to guide functional activities and ensures adherence to all Toxicology and Pathology SOPs
  • Maintain current knowledge of regulatory guidance, industry standards and recommendations
  • Participates in selecting, developing and evaluating personnel to ensure efficient operation within the histopathology group
  • Other pathology and translational medicine-related tasks as assigned
Minimum Requirements
  • DVM with 6+ years of post-graduate experience in a pharmaceutical, biotech or academic organization
  • Board certification in Veterinary Pathology (DACVP or ECVP)
  • Previous experience working on programs that integrate pathological results to drive clinical development
  • Experience with LIMS, digital/computational pathology platforms to characterize features from H&E and IHC images
  • Expert knowledge in nonclinical safety assessment in drug development of small molecules, biologics, and peptides. Knowledge in gene therapy is plus
  • Proven project management skills with the ability to manage multiple projects and priorities simultaneously
  • Excellent communication skills (both oral and written) and collaboration skills with the ability to work effectively in a fast paced cross-functional team environment
  • Deep understanding of regulatory requirements for nonclinical safety assessments, including experience with FDA, EMA, and other global health authorities
  • Experience in responding to regulatory questions including discussion documents for various Health Authorities in support of discovery and development programs
Preferred Education, Experience and Skills
  • Master's or PhD in a scientific discipline

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 talent@askbio.com.