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 ...
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 ...
Experience in Cell & Gene Therapy (CGT), including CAR-T, gene editing, or other advanced therapies, is strongly preferred. As a trusted partner to our customers, you will lead high-profile programs ...
Experience in Cell & Gene Therapy (CGT), including CAR-T, gene editing, or other advanced therapies, is strongly preferred. As a trusted partner to our customers, you will lead high-profile programs ...
Project Manager I - Cell & Gene Therapy (Sponsor Dedicated) Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with ...
Project Manager I - Cell & Gene Therapy (Sponsor Dedicated) Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with ...
Clinical Project Management Director, Cell & Gene Therapy - Global Study Leadership
Durham, NC · On-site
$77K - $105K/yr
Experience in Cell & Gene Therapy (CGT), including CAR-T, gene editing, or other advanced therapies, is strongly preferred. As a trusted partner to our customers, you will lead high-profile programs ...
Clinical Project Management Director, Cell & Gene Therapy - Global Study Leadership
Durham, NC · On-site
$77K - $105K/yr
Experience in Cell & Gene Therapy (CGT), including CAR-T, gene editing, or other advanced therapies, is strongly preferred. As a trusted partner to our customers, you will lead high-profile programs ...
Clinical Project Management Director, Cell & Gene Therapy - Global Study Leadership
Durham, NC · On-site
$77K - $105K/yr
Experience in Cell & Gene Therapy (CGT), including CAR-T, gene editing or other advanced therapies, is strongly preferred. As a trusted partner to our customers, you will lead high-profile programs ...
Clinical Project Management Director, Cell & Gene Therapy - Global Study Leadership
Durham, NC · On-site
$77K - $105K/yr
Experience in Cell & Gene Therapy (CGT), including CAR-T, gene editing or other advanced therapies, is strongly preferred. As a trusted partner to our customers, you will lead high-profile programs ...
Role Overview The Advanced Therapy Social Work Coordinator serves as a dedicated patient and caregiver advocate within The Duke Cell and Gene Therapy Center, ensuring that patients can access ...
Quick apply
Role Overview The Advanced Therapy Social Work Coordinator serves as a dedicated patient and caregiver advocate within The Duke Cell and Gene Therapy Center, ensuring that patients can access ...
Manufacturing Engineer - Gene Therapy Production
Morrisville, NC · On-site
$68K - $87K/yr
We are seeking a mission-driven Manufacturing Engineer to execute critical production runs across both cGMP and non-cGMP Gene Therapy campaigns. This role offers a unique opportunity to contribute to ...
Manufacturing Engineer - Gene Therapy Production
Morrisville, NC · On-site
$68K - $87K/yr
We are seeking a mission-driven Manufacturing Engineer to execute critical production runs across both cGMP and non-cGMP Gene Therapy campaigns. This role offers a unique opportunity to contribute to ...
Manufacturing Associate
Cary, NC · On-site
Pay Rate Low: 38 | Pay Rate High: 40 Opportunity to join a cutting edge biotech organization developing innovative gene therapies that enable precise, durable, and scalable treatments for genetic ...
Manufacturing Associate
Cary, NC · On-site
Pay Rate Low: 38 | Pay Rate High: 40 Opportunity to join a cutting edge biotech organization developing innovative gene therapies that enable precise, durable, and scalable treatments for genetic ...
Manufacturing Engineer - Gene Therapy Production
Morrisville, NC · On-site
$68K - $87K/yr
We are seeking a mission-driven Manufacturing Engineer to execute critical production runs across both cGMP and non-cGMP Gene Therapy campaigns. This role offers a unique opportunity to contribute to ...
Quick apply
Manufacturing Engineer - Gene Therapy Production
Morrisville, NC · On-site
$68K - $87K/yr
We are seeking a mission-driven Manufacturing Engineer to execute critical production runs across both cGMP and non-cGMP Gene Therapy campaigns. This role offers a unique opportunity to contribute to ...
The Associate Director / Director, CMC Regulatory Affairs will lead global CMC regulatory strategy and execution for the company's gene therapy programs from early research through clinical ...
Quick apply
The Associate Director / Director, CMC Regulatory Affairs will lead global CMC regulatory strategy and execution for the company's gene therapy programs from early research through clinical ...
Associate Director or Director, CMC Regulatory Affairs
Durham, NC · On-site
$180 - $260/hr
Develop and implement global CMC regulatory strategies for gene therapy programs from early development through clinical stages and commercialization. * Provide regulatory guidance on viral vector ...
Associate Director or Director, CMC Regulatory Affairs
Durham, NC · On-site
$180 - $260/hr
Develop and implement global CMC regulatory strategies for gene therapy programs from early development through clinical stages and commercialization. * Provide regulatory guidance on viral vector ...
The Associate Director / Director, CMC Regulatory Affairs will lead global CMC regulatory strategy and execution for the companys gene therapy programs from early research through clinical ...
Quick apply
The Associate Director / Director, CMC Regulatory Affairs will lead global CMC regulatory strategy and execution for the companys gene therapy programs from early research through clinical ...
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 ...
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 ...
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 ...
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 ...
This role requires strong experience in regulatory strategy for biologics or gene therapies and the ability to work cross-functionally with clinical development, clinical operations, nonclinical, ...
Quick apply
This role requires strong experience in regulatory strategy for biologics or gene therapies and the ability to work cross-functionally with clinical development, clinical operations, nonclinical, ...
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 ...
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 ...
Significant experience operating within clinical and commercial cGMP manufacturing environments, ideally within gene therapy, viral vectors, cell therapy, biologics, or other advanced therapy ...
Significant experience operating within clinical and commercial cGMP manufacturing environments, ideally within gene therapy, viral vectors, cell therapy, biologics, or other advanced therapy ...
Significant experience operating within clinical and commercial cGMP manufacturing environments, ideally within gene therapy, viral vectors, cell therapy, biologics, or other advanced therapy ...
Significant experience operating within clinical and commercial cGMP manufacturing environments, ideally within gene therapy, viral vectors, cell therapy, biologics, or other advanced therapy ...
The Gene Therapy Center established itself as an international leader in the development of Adeno-associated Virus (AAV) vector technology and AAV gene therapy approaches. The AAV technology that was ...
The Gene Therapy Center established itself as an international leader in the development of Adeno-associated Virus (AAV) vector technology and AAV gene therapy approaches. The AAV technology that was ...
Gene Therapy information
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$11.22 - $13.83
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$17.72 is the 25th percentile. Wages below this are outliers.
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The median wage is $20.52 / hr.
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$11
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$39
How much do gene therapy jobs pay per hour?
What are the key skills and qualifications needed to thrive in gene therapy roles?
What is gene therapy and how does it work?
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?
| Aspect | Gene Therapy | Clinical Research Coordinator |
|---|---|---|
| Required Credentials | Advanced degrees in genetics, molecular biology, or related fields; specialized training in gene editing techniques | Bachelor's degree in health sciences, biology, or related fields; certification often preferred |
| Work Environment | Laboratories, biotech companies, hospitals conducting gene therapy research | Clinical trial sites, hospitals, research institutions overseeing patient studies |
| Employer & Industry Usage | Biotech firms, pharmaceutical companies, academic research centers | Hospitals, 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?
What can you do with gene therapy?

Full-time
Re-posted 11 days ago
IQVIA rating
8.1
Based on 53 frontline employees who took The Breakroom Quiz
60th of 221 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.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