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How much do gene therapy jobs pay per hour?

As of Jul 13, 2026, the average hourly pay for gene therapy in the United States is $23.91, according to ZipRecruiter salary data. Most workers in this role earn between $18.27 and $26.44 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in Gene Therapy roles, and why are they important?

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 is the highest paying job in genetics?

In genetics, roles such as genetic counselors, research directors, and clinical geneticists tend to have the highest salaries, often exceeding $150,000 annually. Senior positions requiring advanced degrees, specialized skills, and leadership responsibilities typically offer the highest compensation in the field.

What career does gene therapy have?

A career in gene therapy involves working as a researcher, scientist, or clinician focused on developing and applying gene-based treatments for diseases. Professionals typically have backgrounds in molecular biology, genetics, or biomedical sciences and may work in laboratories, hospitals, or biotech companies. Skills in laboratory techniques, data analysis, and regulatory compliance are important in this field.

What biology jobs pay over $100k?

In the field of gene therapy, roles such as senior research scientist, clinical development director, and regulatory affairs manager often have salaries exceeding $100,000 annually. These positions typically require advanced degrees, specialized skills in molecular biology or genetics, and experience with clinical trials or regulatory processes.
More about Gene Therapy jobs
What cities are hiring for Gene Therapy jobs? Cities with the most Gene Therapy job openings:
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Gene Therapy jobs near you
Infographic showing various Gene Therapy job openings in the United States as of July 2026, with employment types broken down into 3% Locum Tenens, 2% As Needed, 75% Full Time, 17% Part Time, 1% Temporary, and 2% Contract. Highlights an 77% Physical, 1% Hybrid, and 22% Remote job distribution, with an average salary of $49,724 per year, or $23.9 per hour.
Senior Medical Director- Cell and Gene Therapy

Senior Medical Director- Cell and Gene Therapy

IQVIA

Durham, NC • Remote

Full-time

Re-posted 18 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

55th of 210 rated it services

Job description

Job Overview

The IQVIA Cell and Gene Therapy Center of Excellence (CAGT COE), a hub of CAGT clinical innovation, is growing! We are looking for an exceptional Board-Certified physician to join our team as a Medical Strategy Lead to help us expand our CAGT portfolio, with an emphasis on Gene Therapy/Gene Editing platforms, and advance this dynamic and rapidly expanding area of clinical development.The CAGT Medical Strategy Lead is a subject matter expert with experience in clinical research and clinical trials in CAGT and especially in the areas of Gene Therapy/Gene Editing, who will be a champion for CAGT across IQVIA.The key remit of the role is drive growth of the IQVIA CAGT portfolio through scientific and clinical expertise. The CAGT Medical Strategy Lead will be charged with using his/her clinical, scientific, and operational knowledge to harness the vast IQVIA data and clinical trial resources to develop innovative, data-driven, and patient-centered solutions for CAGT trials.The CAGT Medical Strategy Lead will provide clinical and scientific expertise to all IQVIA divisions as requested and will collaborate closely with indication-specific teams to develop integrated strategies for CAGT clinical trials and studies.The CAGT Medical Strategy Lead will also be responsible for early engagement business development activities, providing scientific knowledge and expertise to guide sponsors in CAGT development. As a subject matter expert in CAGT, the CAGT Medical Strategy Lead will drive thought leadership activities including presentations, publications, and interactions with the medical scientific community.

Responsibilities

  • Accountable and responsible for creating innovative, evidence-based, and patient-centered delivery strategies and solutions for CAGT trials or studies, addressing the specific needs and challenges of each customer.

  • In partnership with indication-specific Medical Strategy, Operations, Sales, and other functions, responsible for award of strategic and tactical new business to achieve annual Gross New Business targets.

  • Responsible for the inclusion of CAGT elements into proposals.

  • Provide scientific, clinical, and operational advice to internal stakeholders developing proposals: this may include, but is not limited to, providing the strategy to protocol design/clinical development plan, mining data to address important clinical questions relevant to the study, reviewing the protocol for scientific/regulatory soundness and feasibility, logistics challenges, identification of target site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape.

  • Support preparation of customer and bid defense meetings, e.g. training and preparation of the assigned project team; provide specific content; ensure presentation focus and content effectively conveys CAGT strategy.

  • Attends and presents at customer meeting, or bid defense or partnership meetings, as required.

  • Participates in strategic business development activities including presentations to prospective clients and professional meetings.

  • Maintains awareness of industry pipeline and scientific and business landscape; supports due diligence research of the CAGT landscape.

  • Leads CAGT thought leadership at IQVIA which may include publications, presentations, and taking a leadership role in scientific activities.

Qualifications

  • A physician (MD or DO) or physician/scientist (MD/PhD) with experience in CAGT and especially in gene therapy/gene editing.

  • A degree from an accredited and internationally recognized school is required.

  • Certification in any medical sub-specialty will be considered and preference will be given to candidates with formal training in Neurology, Medical Genetics, or Cardiology.

  • Highly qualified and experienced candidates with other terminal degrees such as a PhD or Pharm D will also be considered.

  • At least 5 years clinical research relevant experience, including hands on operational delivery and/or drug development experience in gene therapy/gene editing.

  • Robust and current knowledge of scientific, clinical, regulatory, commercial and competitive landscape in CAGT, especially in gene therapy/gene editing.

  • Excellent skills in providing consultation and advice on multiple assignments are required, as well as initiative and flexibility.

  • In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; e.g. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

  • Demonstrated ability to understand customer needs, have difficult conversations with internal/external stakeholders and customers, negotiate solutions and understand impacts on the overall offering.

  • Strong clinical research skills and commitment to evidence-based and patient-centered clinical development.

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IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $186,300.00 - $519,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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About IQVIA

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At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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