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Remote Gene Editing Jobs (NOW HIRING)

This position reports to the Vice President, Gene Editing Therapeutics and is part of the Gene Editing Business Unit and will be fully remote . In this role, you will have the opportunity to:

This position reports to the Vice President, Gene Editing Therapeutics and is part of the Gene Editing Business Unit and will be fully remote . In this role, you will have the opportunity to:

This position reports to the Vice President, Gene Editing Therapeutics and is part of the Gene Editing Business Unit and will be fully remote . In this role, you will have the opportunity to:

Job Title Product Applications Specialist Location(s) US Remote - IL, US Remote - IN, US Remote ... Dharmacon's services and reagents, which leverage gene-editing and modulation technologies, are now ...

Business Development Manager

Boston, MA ยท On-site +1

$145K - $175K/yr

... remote. You will be a part of the North American Sales Team and report to the Regional Sales ... gene editing, DNA plasmids, mRNA therapeutics, viral vector technologies, CAR-T, etc. * At least 1 ...

Business Development Manager

Boston, MA ยท On-site +1

$145K - $175K/yr

... remote. You will be a part of the North American Sales Team and report to the Regional Sales ... gene editing, DNA plasmids, mRNA therapeutics, viral vector technologies, CAR-T, etc. * At least 1 ...

... gene editing and application technologies to provide nitrogen to crops. We are dedicated to ... Remote based - based upon territory supported. Travel Required This position will require travel 80 ...

Territory Sales Manager - Heartland

Madison, WI ยท On-site +1

$77K - $96K/yr

... gene editing and application technologies to provide nitrogen to crops. We are dedicated to ... Remote based - based upon territory supported. Travel Required This position will require travel 80 ...

Associate Editor

Manhattan, NY ยท On-site +1

$60K - $65K/yr

Experience with line and developmental editing, project managing frontlist fiction, and working ... This position is classified as remote but is tied to our New York, NY office located at 120 ...

... gene editing and application technologies to provide nitrogen to crops. We are dedicated to ... Exciting opportunity to work with a talented and fun team #LI-Remote

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Remote Gene Editing information

See salary details

$37K

$84.5K

$130K

How much do remote gene editing jobs pay per year?

As of Sep 14, 2026, the average yearly pay for remote gene editing in the United States is $84,537.00, according to ZipRecruiter salary data. Most workers in this role earn between $65,000.00 and $101,500.00 per year, depending on experience, location, and employer.

What is remote gene editing?

A remote gene editing job involves working from a location outside of a traditional lab or office to design, analyze, or manage gene editing projects. These roles often utilize digital tools for data analysis, project management, and collaboration with research teams. Responsibilities may include designing genetic experiments, analyzing DNA sequences, or supporting clients with gene editing technologies like CRISPR. Most remote positions require a strong background in genetics, bioinformatics, or molecular biology, as well as experience with relevant software and databases.

What are the key skills and qualifications needed to thrive in remote gene editing?

To thrive as a Remote Gene Editing Specialist, you need a strong background in molecular biology, genetics, and bioinformatics, typically supported by an advanced degree in a life science field. Familiarity with CRISPR/Cas9 or other gene editing technologies, laboratory information management systems (LIMS), and relevant certifications such as GLP/GMP are essential. Strong problem-solving abilities, attention to detail, and effective communication skills help you collaborate with remote teams and ensure the accuracy of experimental outcomes. These combined skills enable safe, precise, and compliant gene editing work, especially in distributed or virtual lab environments.

What are some common challenges faced by professionals working in remote gene editing roles, and how can they be addressed?

Professionals in remote gene editing roles often encounter challenges such as coordinating complex experiments across distributed teams, managing sensitive data securely, and ensuring access to necessary lab resources when working off-site. To address these, clear communication protocols, utilization of secure cloud-based data platforms, and regular virtual check-ins with lab partners are essential. Additionally, staying updated with current gene editing technologies and remote collaboration tools helps maintain efficiency and data integrity in a remote environment.

What is the difference between Remote Gene Editing vs Remote Genetic Counselor?

AspectRemote Gene EditingRemote Genetic Counselor
Required CredentialsAdvanced degrees in genetics, molecular biology, or related fields; specialized training in gene editing techniquesMaster's degree in genetics, genetic counseling, or related health sciences; certification (e.g., ABGC)
Work EnvironmentLaboratories, research institutions, biotech companies, often collaborative and technicalHealthcare settings, clinics, telehealth platforms, patient-focused
Industry UsageBiotech, research, gene therapy developmentHealthcare, clinical genetics, patient counseling

Remote Gene Editing involves working on developing and applying gene editing technologies like CRISPR, often in research or biotech settings. Remote Genetic Counselors focus on advising patients about genetic risks and testing options. While both roles require genetics knowledge, gene editing is more technical and research-oriented, whereas genetic counseling is patient-centered and clinical.

More about Remote Gene Editing jobs

What cities are hiring for Remote Gene Editing jobs?

Cities with the most Remote Gene Editing job openings:

What are the most commonly searched types of Gene Editing jobs?

The most popular types of Gene Editing jobs are:

What states have the most Remote Gene Editing jobs?

States with the most job openings for Remote Gene Editing jobs include:

What other helpful pages are available for Remote Gene Editing?

Other pages related to Remote Gene Editing:

Infographic showing various Remote Gene Editing job openings in the United States as of September 2026, with employment types broken down into 2% Internship, 77% Full Time, 17% Part Time, 1% Temporary, and 3% Contract. Highlights an 68% Physical, 5% Hybrid, and 27% Remote job distribution, with an average salary of $84,537 per year, or $40.6 per hour.

Sr. Scientist, Gene Editing Materials Process Development(temp)

South San Francisco, CA โ€ข On-site, Remote

Allogene Therapeutics
Biotechnology Research and Developmentย โ€ขย 201 - 500 employees

$60 - $70/hr

Contractor

Re-posted 7 days ago


Key responsibilities

  • Support CDMOs in process development and process characterization of gene editing and/or gene delivery materials.

  • Collaborate with internal and external teams to ensure alignment and assess impacts of process and method changes.

  • Assist in planning, executing, and troubleshooting deviations during process development and GMP manufacturing runs.


Job description

Job Description
About Allogene:
Allogene Therapeutics, with headquarters in South San Francisco, is a clinical-stage biotechnology company pioneering the development of allogeneic chimeric antigen receptor T cell (AlloCAR T) products for cancer and autoimmune disease. Led by a management team with significant experience in cell therapy, Allogene is developing a pipeline of "off-the-shelf" CAR T cell product candidates with the goal of delivering readily available cell therapy on-demand, more reliably, and at greater scale to more patients.
Job Description:
We are seeking a highly motivated, self-driven and collaborative individual to join the Process and Product Development organization. The successful candidate will serve as a technical lead working with internal teams and external CDMOs focused on development and continued improvement of the manufacturing processes of gene delivery and/or gene editing materials used in allogeneic cell therapies. This individual will provide technical leadership across the product lifecycle, from early-stage process development through late-stage process characterization, control strategy development and commercial manufacturing readiness to support BLA submission and commercialization. This position will also provide technical oversight to support the production and re-supply of gene delivery and gene editing materials, as appropriate. This position can be remote with some travel to San Francisco and various CDMO sites.
Responsibilities include, but are not limited to:
  • Serve as technical subject matter expertise supporting CDMOs to provide process development expertise for gene editing and/or gene delivery materials
  • Partner with internal and external R&D, External Manufacturing, MSAT, and Quality to ensure cross-functional alignment
  • Contribute to process development, process characterization, control strategy development and PPQ planning activities
  • Work with internal and external partners to assess impact to process and method change for gene editing and/or gene delivery materials
  • Support planning, execution and troubleshooting deviations of Process Development and GMP runs at CDMOs
  • Assess impact of gene editing and/or gene delivery materials on CART production process
  • Engage with broader Process and Product Development team to contribute to achievement of Department goals
  • Other duties as assigned

Position Requirements & Experience:
  • PhD in biological sciences, engineering or related discipline with 5+ years of relevant experience in process development for the manufacturing of gene and cell therapy or related field is required (or MS with 10+ years, BS with 12+ years of industry experience)
  • Strong knowledge background and direct experience developing, characterizing, scaling, or supporting GMP manufacturing processes for gene editing materials (e.g., mRNA, nucleases) and/or gene delivery materials (e.g., AAV, lentiviral vectors, non-viral delivery systems) is strongly preferred. Experience solely using these materials for gene editing applications without involvement in process development or manufacturing is unlikely to meet the requirements of this role.
  • Experience with applying Design of Experiments (DOE), statistical analysis, and data visualization tools (JMP, Spotfire, or equivalent) for process development or characterization studies
  • Prior experience serving as technical support for internal and external teams to manage process development and manufacturing at CDMOs is a plus
  • Experience with analytical assay development, qualification, transfer is a plus
  • Familiarity with cGMP manufacturing and regulatory expectations for biologics gene editing material or cell therapy products is a plus
  • Strong interpersonal skills including verbal and written communication are essential in this collaborative work environment
  • Ability to work independently and in a matrixed environment
  • Excellent organizational skills and an ability to prioritize effectively to deliver results within reasonably established timelines
  • Ability to travel up to 10%
  • Candidates must be authorized to work in the U.S
  • This is a 1-year contract opportunity with the possibility of extension or contract-to-hire.

We offer a chance to work with talented people in a collaborative environment. The expected hourly range for this role is $60 to $70 per hour. Actual pay will be determined based on experience, qualifications, geographic location, business needs, and other job-related factors permitted by law.
As an equal opportunity employer, Allogene is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state and local laws. We also embrace differences in experience and background, and welcome diversity of opinions and thought with active recruitment and internships designed to create a stronger and better Allogene that is focused on developing life-changing products for patients.
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