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Associate Director Gene Editing Jobs (NOW HIRING)

The Director will be responsible for establishing robust organoid and gene editing workflows that directly support investigator needs, building standardized and scalable operating procedures ...

Postdoctoral associate will also run assays to assess editing outcomes and assess immune response to gene editing reagents. This position offers a unique opportunity exposed to cutting edge ...

... gene editing, and/or life science industry understanding * Influencing all levels of an organization including Senior and Functional Leaders to lead change without direct supervisory leverage.

... gene editing, and/or life science industry understanding * Influencing all levels of an organization including Senior and Functional Leaders to lead change without direct supervisory leverage.

... gene editing, and/or life science industry understanding * Influencing all levels of an organization including Senior and Functional Leaders to lead change without direct supervisory leverage.

... gene editing, and/or life science industry understanding * Influencing all levels of an organization including Senior and Functional Leaders to lead change without direct supervisory leverage.

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Associate Director Gene Editing information

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$30.5K

$102.7K

$173K

How much do associate director gene editing jobs pay per year?

As of Sep 9, 2026, the average yearly pay for associate director gene editing in the United States is $102,728.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,000.00 and $141,000.00 per year, depending on experience, location, and employer.

What does an associate director gene editing do?

An Associate Director of Gene Editing is responsible for overseeing gene editing projects and teams within a biotechnology or pharmaceutical organization. They design and lead research strategies, ensure compliance with regulatory standards, and collaborate with cross-functional teams to drive innovation in gene editing technologies such as CRISPR. Their role includes managing budgets, mentoring scientists, and contributing to scientific publications and presentations. The Associate Director plays a key role in advancing gene editing programs from discovery through preclinical and sometimes early clinical development.

What are the main challenges faced by an associate director gene editing when leading cross-functional scientific teams?

As an Associate Director of Gene Editing, one common challenge is aligning the scientific goals of diverse teams, such as research scientists, bioinformaticians, and regulatory experts, to drive complex gene editing projects forward. Balancing innovative research with the practicalities of regulatory compliance and tight timelines can be demanding. Effective communication and project management skills are crucial for navigating differing priorities and ensuring seamless collaboration across departments. Additionally, staying abreast of rapidly evolving gene editing technologies requires continuous learning and adaptability.

What are the key skills and qualifications needed to thrive as an associate director gene editing, and why are they important?

To excel as an Associate Director Gene Editing, you need advanced expertise in molecular biology, gene editing technologies (such as CRISPR/Cas9), and a PhD or equivalent experience in a related scientific field. Familiarity with laboratory automation, bioinformatics tools, and regulatory compliance systems is typically required, often supplemented by certifications in GLP or GCP. Leadership, strategic thinking, and strong communication are important soft skills for managing teams and collaborating across departments. These abilities ensure effective project execution, innovation, and adherence to industry standards in the rapidly evolving field of gene editing.

What are popular job titles related to Associate Director Gene Editing jobs?

For Associate Director Gene Editing jobs, the most frequently searched job titles are:

Infographic showing various Associate Director Gene Editing job openings in the United States as of June 2026, with employment types broken down into 50% Temporary, and 50% Contract. Highlights an 81% Physical, 1% Hybrid, and 18% Remote job distribution, with an average salary of $102,728 per year, or $49.4 per hour.

GSOM Director-Organoid Facility

New York, NY • On-site

NYULMC
Hospitals • 501 - 1,000 employees

Full-time

Medical, Retirement

Re-posted 13 days ago


NYU Langone Health rating

8.4

Company rating: 8.4 out of 10

Based on 250 frontline employees who took The Breakroom Quiz

22nd of 898 rated healthcare providers


Job description


NYU Grossman School of Medicine is one of the nation's top-ranked medical schools. For 175 years, NYU Grossman School of Medicine has trained thousands of physicians and scientists who have helped to shape the course of medical history and enrich the lives of countless people. An integral part of NYU Langone Health, the Grossman School of Medicine at its core is committed to improving the human condition through medical education, scientific research, and direct patient care. At NYU Langone Health, equity and inclusion are fundamental values. We strive to be a place where our exceptionally talented faculty, staff, and students of all identities can thrive. We embrace inclusion and individual skills, ideas, and knowledge.
For more information, go to med.nyu.edu, and interact with us on LinkedIn, Glassdoor, Indeed, Facebook, X and Instagram.
Position Summary:
We have an exciting opportunity to join our team as a GSOM Director-Organoid Facility.
The Institute for Regenerative Medicine seeks an accomplished and collaborative Director to lead the development, implementation, and expansion of a state-of-the-art organoid core. The Director will be responsible for establishing robust organoid and gene editing workflows that directly support investigator needs, building standardized and scalable operating procedures, ensuring rigorous quality control, and expanding facility capabilities over time. This role will require close partnership with faculty, laboratory personnel, and institutional core facilities to create a highly responsive, efficient, and scientifically rigorous resource that advances regenerative medicine.
Job Responsibilities:
1. Establish and implement foundational organoid platforms
Work closely with the initial group of priority investigators to assess and meet their organoid-related research needs.
Establish organoid protocols for at least one lineage derived from each of the three germ layers.
Develop these three germ layer organoid systems in parallel to build broad foundational capability efficiently.
Interface directly with individual laboratories to ensure protocols are optimized for their scientific and experimental needs.
Translate laboratory-specific SOPs into standardized Core SOPs that support reproducibility, scalability, and shared facility operations.
Implement all necessary cell line tracking, documentation, and quality control procedures to support rigorous and reliable core operations.
2. Build gene editing capabilities within the facility
Obtain and evaluate gene editing protocols from key internal and external collaborators.
Work directly with relevant laboratory personnel, including postdoctoral fellows, to adapt and refine protocols for facility implementation.
Engage with high-performing external gene editing programs to identify operational best practices and efficient models that could inform facility development.
Establish gene editing workflows that can be deployed in support of investigator projects.
Finalize standardized SOPs for gene editing services within the facility.
Partner with the NYU Genome Engineering Core to explore opportunities for cross-training personnel and leveraging existing institutional expertise and resources.
3. Introduce automation to enhance throughput and efficiency
After the needs of the initial faculty users have been successfully met and foundational workflows are operating effectively, identify opportunities to introduce automation into high-throughput processes.
Develop automation strategies for applications such as qPCR workflows, 96-well organoid generation, and other scalable processes as appropriate.
Evaluate and implement technologies that improve efficiency, reproducibility, and capacity while maintaining high scientific quality.
4. Expand facility services and institutional engagement
Broaden the facility's service offerings to support additional investigators across NYULH.
Develop and implement regular training programs for users, including faculty, trainees, and research staff.
Promote best practices in organoid culture, gene editing, quality control, and experimental reproducibility.
Serve as a scientific and operational resource for the institutional research community in organoid model development and related technologies
Minimum Qualifications:
To qualify you must have a PhD, MD/PhD, or equivalent in stem cell biology, developmental biology, regenerative medicine, cell biology, bioengineering, or a related field.
Significant experience developing and implementing organoid culture systems.
Demonstrated expertise in SOP development, laboratory standardization, and quality control systems. Prior experience in establishing similar facilities highly desirable.
Experience with genome engineering and gene editing platforms, including adapting protocols for shared-resource or core settings.
Strong understanding of cell line tracking, QC documentation, and reproducibility standards.
Experience working collaboratively with faculty and research teams in a service-oriented environment.
Familiarity with laboratory automation and high-throughput workflows is highly desirable.
Excellent interpersonal, organizational, communication, and leadership skills.
Qualified candidates must be able to effectively communicate with all levels of the organization.
NYU Grossman School of Medicine provides its staff with far more than just a place to work. Rather, we are an institution you can be proud of, an institution where you'll feel good about devoting your time and your talents. At NYU Langone Health, we are committed to supporting our workforce and their loved ones with a comprehensive benefits and wellness package. Our offerings provide a robust support system for any stage of life, whether it's developing your career, starting a family, or saving for retirement. The support employees receive goes beyond a standard benefit offering, where employees have access to financial security benefits, a generous time-off program and employee resources groups for peer support. Additionally, all employees have access to our holistic employee wellness program, which focuses on seven key areas of well-being: physical, mental, nutritional, sleep, social, financial, and preventive care. The benefits and wellness package is designed to allow you to focus on what truly matters. Join us and experience the extensive resources and services designed to enhance your overall quality of life for you and your family.
NYU Grossman School of Medicine is an equal opportunity employer and committed to inclusion in all aspects of recruiting and employment. All qualified individuals are encouraged to apply and will receive consideration. We require applications to be completed online.
View Know Your Rights: Workplace discrimination is illegal.
NYU Langone Health provides a salary range to comply with the New York state Law on Salary Transparency in Job Advertisements. The salary range for the role is $121,792.22 - $$200,000.00 Annually. Actual salaries depend on a variety of factors, including experience, specialty, education, and hospital need. The salary range or contractual rate listed does not include bonuses/incentive, differential pay or other forms of compensation or benefits.
To view the Pay Transparency Notice, please click here

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