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Gene Editing Jobs (NOW HIRING)

The successful candidate will support the maintenance and gene editing of bovine cell lines, prepare critical reagents, and contribute to the development, optimization, and documentation of protocols ...

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Gene Editing information

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$35K

$71.8K

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How much do gene editing jobs pay per year?

As of Jun 7, 2026, the average yearly pay for gene editing in the United States is $71,789.00, according to ZipRecruiter salary data. Most workers in this role earn between $54,500.00 and $85,000.00 per year, depending on experience, location, and employer.

What are some typical daily tasks and responsibilities in a Gene Editing role?

Professionals in Gene Editing roles often spend their days designing and executing experiments, analyzing genetic sequences, and developing new methods for modifying DNA in various organisms. You may also be responsible for maintaining detailed lab documentation, troubleshooting experimental challenges, and collaborating with interdisciplinary teams of biologists, chemists, and data analysts. Common tasks include preparing genetic constructs, operating advanced laboratory equipment, and interpreting research results to inform ongoing projects. These responsibilities are integral to driving scientific discovery and bringing new gene-editing applications to practical use.

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

To thrive in Gene Editing, you need a strong background in molecular biology, genetics, and biotechnology, typically supported by an advanced degree such as a PhD or MS in related fields. Familiarity with gene editing tools like CRISPR-Cas9, PCR, DNA sequencing platforms, and relevant software is essential, along with potential certifications in laboratory safety or bioinformatics. Attention to detail, strong problem-solving abilities, and collaborative communication skills are valuable for navigating complex experiments and coordinating with research teams. These competencies are vital to ensure experimental accuracy, maintain compliance with regulations, and drive innovation in this rapidly evolving scientific area.

What is a Gene Editing job?

A Gene Editing job involves researching, developing, and applying techniques to modify DNA in organisms to achieve desired traits or correct genetic defects. Professionals in this field work with technologies like CRISPR, TALENs, and zinc finger nucleases to edit genes for medical, agricultural, or scientific purposes. Roles may include laboratory research, therapeutic development, or regulatory compliance. Scientists in this field typically have backgrounds in genetics, molecular biology, or biotechnology.

More about Gene Editing jobs
What cities are hiring for Gene Editing jobs? Cities with the most 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 Gene Editing jobs? States with the most job openings for Gene Editing jobs include:
Associate Vice President, Regulatory Strategy

Associate Vice President, Regulatory Strategy

Lilly

Boston, MA

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 14 days ago


Eli Lilly and Company rating

8.8

Company rating: 8.8 out of 10

Based on 62 frontline employees who took The Breakroom Quiz

11th of 71 rated pharmaceutical


Job description

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world.

Organization Overview:

Verve Therapeutics, a wholly owned subsidiary of Eli Lilly & Company, is a clinical-stage genetic medicines company established with a mission to solve the global health epidemic of cardiovascular disease. Founded by world-leading experts in cardiovascular medicine, human genetics and gene-editing, Verve is pioneering a new approach to the care of cardiovascular disease, potentially transforming treatment from chronic management to single-course gene editing medicines.

Responsibilities:

The Associate Vice President, Regulatory Strategy will provide strategic regulatory leadership for the advancement of our gene editing therapies. This leader will be responsible for overseeing development and implementation of advanced global regulatory strategies as well as the day-to-day management of regulatory activities to support multiple early-stage global programs. This role requires deep regulatory expertise, strong scientific competence, and the ability to lead through complexity in a fast-paced, innovation-focused environment.

  • Lead and develop a team of leaders, fostering a culture of accountability, inclusion, and high performance
  • Maintain oversight of regulatory activities including but not limited to clinical trial applications, IND amendments, annual reports, safety reporting, expedited program applications, and meetings with global health authorities
  • Provide strategic regulatory input into content of relevant sections of project/product specific documents submitted to global regulatory agencies and ensure that these documents meet high scientific standards and regulatory requirements
  • Provide leadership to resolve critical regulatory issues and bring the appropriate partners and regulatory experts together as needed
  • Support Global Regulatory Lead(s) in providing robust regulatory advice and plans to the various project teams to ensure that the business needs are in compliance with regulations and/or regulatory advice received from the agencies
  • Coach and mentor direct reports, investing in their professional growth and building leadership capability across the organization
  • Monitor the development of new regulatory requirements or guidance documents and regulatory precedent to advise product teams of any impact on the business or development programs and to ensure alignment with evolving regulatory requirements in the gene editing space
  • Build and maintain strong relationships with cross-functional teams as well as senior leadership

Basic Requirements:

  • Advanced degree in biology, chemistry or closely related field
  • 15+ years of relevant industry experience with roles of increasing responsibility and scope

Additional Skills/Preferences:

  • PhD or PharmD strongly preferred
  • Previous experience with complex biologics, genetic editing, or gene therapy products
  • Prior experience in a scientific and/or technical setting to allow understanding of experiments, documentation and data
  • Ability to take broad abstract concepts and distill them down into a vision with an actionable plan
  • Ability to apply critical thinking to foreshadow and resolve challenges and roadblocks to allow the organization to push forward
  • Ability to analyze data to drive conceptual thinking and decision making
  • Excellent written and verbal communication skills, exceptional listening skills, strong presentation skills, and good negotiating and influencing skills

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.


Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.

Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is

$267,000 - $391,600

Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

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About Eli Lilly

Sourced by ZipRecruiter

Eli Lilly, based in Indianapolis, IN, US, is one of the pioneers in the pharmaceutical industry with a rich history dating back to 1876. This global pharmaceutical company focuses on discovering, developing, manufacturing and selling pharmaceutical products in approximately 120 countries. The company's product categories include endocrinology, oncology, cardiovascular, neuroscience, and immunology. Having invested over $9 billion in research and development in the past decade, Eli Lilly is also committed to creating high-quality medicines that meet real needs. As a recipient of several awards and recognitions, Eli Lilly is known for its focus on life-saving research and drug development. Their mission is to make medicines that help people live longer, healthier, and more active lives.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Indianapolis, IN, US

Year founded

1876