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PepGen

Regulatory Affairs Co-op

internship•Boston

Summary

Location

Boston

Type

internship

Experience

0-2 years

Company links

WebsiteLinkedInLinkedIn

About this role

The Co-op will support key aspects of regulatory to support the development of PepGen’s clinical stage novel peptide-oligonucleotide conjugate therapeutics for a range of neuromuscular and neurologic indications. In this hands-on regulatory position, the successful candidate will work closely with the Global Regulatory and Medical Writing team and gain exposure and experience in how to develop a global regulatory strategy, including submissions, regulatory compliance, and the understanding and application of guidance and requirements for multiple geographies (including the USA and Canada, and beyond). 

Responsibilities:  

  • With the wider teams, develop planning, logistics, and document development for regulatory agency submissions and interactions including CTA submissions, development of query responses documents, briefing documents for agency interactions and other general regulatory agency submissions, 

  • Support Regulatory Intelligence surveillance and interpretation to aid the development of the global regulatory strategy plans to anticipate regulatory obstacles and emerging issues, including changing regulations, 

  • Support the development of regulatory processes for submission planning and management, and oversight of regulatory requirements. 

Requirements: 

  • Must be an active Northeastern University student pursuing a BS or MS in Biology, Pharmaceutical Sciences, or a closely related field. 

  • Must have excellent interpersonal, written and verbal communication skills, and administrative skills 

  • Excellent computer skills in the following programs: MS Word, PowerPoint, Excel and Project 

  • Ability to work onsite Tuesday – Thursday from 9am to 5pm in the Boston office during the Fall Co-op Cycle (July-Dec 2026)

About PepGen

PepGen is a clinical-stage biotechnology company advancing the next generation of oligonucleotide therapies with the goal of transforming the treatment of severe neuromuscular and neurological diseases. PepGen’s Enhanced Delivery Oligonucleotide (EDO) platform is founded on over a decade of research and development and leverages cell-penetrating peptides to improve the uptake and activity of conjugated oligonucleotide therapeutics. Using these EDO peptides, we are generating a pipeline of oligonucleotide therapeutic candidates designed to target the root cause of serious diseases.

For more information, please visit PepGen.com. Follow PepGen on LinkedIn and X.


EEO Statement
PepGen is an Equal Opportunity Employer committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status.

Recruitment & Staffing Agencies
PepGen does not accept unsolicited agency resumes. The company will not be responsible for any fees related to resumes that are unsolicited. Thank you.

E-Verify

PepGen is an E-Verify Employer. For more information about E-Verify, please see here.

What you'll do

  • The Co-op will support the development of regulatory submissions and interactions, including CTA submissions and query response documents. The candidate will also aid in developing regulatory processes and strategies to anticipate regulatory obstacles.

About PepGen

Driven by our proprietary Enhanced Delivery Oligonucleotide (EDO) platform, we are creating a pipeline of disease-modifying therapeutics with the potential to safely and effectively target the root cause of serious genetic neuromuscular and neurological disorders.

Ready to join PepGen?

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Frequently Asked Questions

What does a Regulatory Affairs Co-op do at PepGen?

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As a Regulatory Affairs Co-op at PepGen, you will: the Co-op will support the development of regulatory submissions and interactions, including CTA submissions and query response documents. The candidate will also aid in developing regulatory processes and strategies to anticipate regulatory obstacles..

Is the Regulatory Affairs Co-op position at PepGen remote?

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The Regulatory Affairs Co-op position at PepGen is based in Boston, Massachusetts, United States. Contact the company through Clera for specific work arrangement details.

How do I apply for the Regulatory Affairs Co-op position at PepGen?

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You can apply for the Regulatory Affairs Co-op position at PepGendirectly through Clera. Click the "Apply Now" button above to start your application. Clera's AI-powered platform will help match your profile with this opportunity and guide you through the application process.
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