Gene Editing Intern

Posted 17 Days Ago
Be an Early Applicant
Durham, NC
Internship
Biotech
The Role
As a Gene Editing Intern at Sarepta, you'll conduct in vitro experiments to advance genetic therapies for neuromuscular diseases, develop disease models, maintain cell cultures, and utilize various molecular biology techniques under the guidance of a Scientist.
Summary Generated by Built In

Why Sarepta? Why Now?

The promise of genetic medicine has arrived, and Sarepta is at the forefront. We hold leadership positions in Duchenne muscular dystrophy (DMD) and limb-girdle muscular dystrophies (LGMDs), and we currently have more than 40 programs in various stages of development in gene therapy, RNA and gene editing. In 2023, we launched our fourth therapy and the first ever gene therapy to treat Duchenne.
 

We’re looking for people who see unlimited potential in themselves and who are motivated by an unwavering commitment to patients.
 

What Sarepta Offers

At Sarepta, we care deeply about all the people in our community and believe in the importance of supporting them in all aspects of their lives. We aspire to maintain a culture that acknowledges people bring their whole selves to work, and we will strive to help everyone in our community integrate their work and personal lives while maintaining productivity.

The Importance of the Role
 

Join our Gene Editing Innovation Center in Durham, North Carolina, as an Intern! You'll conduct groundbreaking in vitro experiments under the guidance of a Scientist, advancing our portfolio of genetic therapies for neuromuscular diseases. This role supports disease modeling operations and develops cutting-edge technologies for research and development.

The Opportunity to Make a Difference

  • Develop 2D and 3D in vitro disease models. 

  • Conduct experiments evaluating novel gene editing, RNA, and gene therapy strategies.

  • Maintain mammalian cell cultures and iPSC differentiations.

  • Perform molecular and cellular biology techniques: transfection, viral transduction, CRISPR-based gene editing, digital PCR, Western blot, cryosectioning, and IF.

  • Implement new methods and technologies for continuous improvement.

  • Troubleshoot routine technical challenges and contribute to their resolution in a timely manner.

  • Participate as part of a team in a laboratory setting contributing to a safe, efficient, and effective work environment.

  • Follow scientific direction to meet project timelines and deliverables.

  • Maintain compliant laboratory documentation and develop technical reports, protocols, and SOPs. 

  • Interpret and present data to internal teams.

  • Perform other related duties as assigned.

More about You

  • Enrolled in a Master’s or PhD program in a scientific field with at least one year of relevant experience: neuromuscular disease, molecular biology, or genetic therapy research.

  • Hands-on experience with 2D/3D in vitro disease models and iPSC culture.

  • Proficiency in mammalian cell line engineering.

  • Skilled in molecular and cellular biology techniques: transfection, viral transduction, CRISPR-based gene editing, digital PCR, Western blot, cryosectioning, and IF.

  • Strong critical thinking and analytical skills.

  • Effective communication skills.

  • Ability to manage multiple projects and adapt to changing priorities.

  • Proficiency with Microsoft Office, GraphPad Prism, gene editing software, and other functional systems.

  • Passion for working in a dynamic, fast-paced team environment and making a difference in the lives of patients.

Join us and be part of a team that's transforming the future of genetic therapies!

Program Timeline:

This application is for a 12-week summer internship program that will start on May 19th and conclude on August 8th, 2025.

What Now?

We’re always looking for solution-oriented, critical thinkers.

So, if you’re comfortable with ambiguity and candor, relish challenging yourself, and place kindness and integrity at the forefront of how you approach your peers and work, then we encourage you to apply.
 

#LI-Onsite#LI-MC1

This position requires work on site at one of Sarepta’s facilities in the United States.

The targeted salary range for this position is $21 - $25 per hour depending upon years of education completed and nature of role.

Candidates must be authorized to work in the U.S.

Sarepta Therapeutics offers a competitive compensation and benefit package.

Sarepta Therapeutics is an Equal Opportunity/Affirmative Action employer and participates in e-Verify.

Top Skills

Gene Editing
Rna
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The Company
HQ: Cambridge, MA
1,464 Employees
On-site Workplace

What We Do

Sarepta Therapeutics, headquartered in Cambridge, Massachusetts, is a global biotechnology company on an urgent mission: engineer precision genetic medicine for rare diseases that devastate lives and cut futures short. We hold leadership positions in Duchenne muscular dystrophy (DMD) and limb-girdle muscular dystrophies (LGMDs), and we currently have more than 40 programs in various stages of development. Our vast pipeline is driven by our multi-platform Precision Genetic Medicine Engine in gene therapy, RNA and gene editing.

For information on our Community Guidelines, please visit sarepta.com/community-guidelines.

We want to share a reminder with all job seekers and candidates regarding the persistence of recruiting fraud. Please read a message about recruiting fraud and steps you can take to protect yourself here: https://www.sarepta.com/recruiting-fraud

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