New · posted Oct 15
Stoke Therapeutics · Biotechnology
Senior Manager, Regulatory Affairs, CMC
- Bedford, MA
- Hybrid
- Full-time
- Manager
Open until filled
The role
The Regulatory CMC Senior Manager is responsible for contributing to the development of Stoke’s products by supporting global CMC regulatory strategies, leading lifecycle management initiatives, and providing regulatory guidance to cross-functional teams for multiple programs. This position will report to the Director of Regulatory CMC.
Interested candidates: Please visit Stoke’s website to learn more and apply directly to the position listed on our Career Center:
What you need
Required Skills & Experience
- BS/ BA degree in scientific, pharmaceutical or engineering discipline; advanced degree preferred
- Minimum of 8 years of industry experience, including a minimum of 5 years directly in CMC Regulatory Affairs
- Direct experience developing and implementing successful regulatory strategies in both US and EU markets
- Direct experience with commercial phase programs and post-approval CMC requirements and implementation of regulatory milestones (e.g., Annual Reports)
- Deep understanding of Module 3 sections and associated ICH, FDA, EMA regulations and guidance documents
- Experience authoring Quality Modules 2.3 and 3; and health authority engagement content (e.g., FDA Briefing Books)
- Practical experience in one of the following areas: manufacturing; process development; validation; analytical development, and/or quality.
- Understanding of technical operations functions and systems including, but not limited to, technical risk assessments, change controls
- Strong oral and written communication skills
- Direct experience with Veeva RIM required
- Preferred Experience:
- Combination Product and/or device experience
- Global (beyond US, EU) regulatory experience
- Working in complex and matrix environments
- Oligonucleotide drug development
What you'll do
- Prepares and executes global regulatory CMC strategy for development programs and future commercial programs, including new applications, information amendments, annual reports, supplements/ variations, and responses to health authority questions.
- Lead author, and able to collaborate with Subject Matter Experts, for Quality Modules. Effectively manage document review and approval workflows.
- Analyzes and interprets technical information for impact to regulatory strategy and decisions
- Assesses change controls for regulatory impact and manages the implementation system for regulatory compliance
- Develops process(es) to track regulatory dossier lifecycle management, health authority questions, and post approval commitments, as needed
- Develops and implements documents, policies, and/or procedures for regulatory operational alignment and efficiencies
- Builds and maintains relationships within the Regulatory Affairs department and Technical Operations (CMC) teams
Pay and benefits
$181,000 – $213,000 a year
Employer providedAt Stoke Therapeutics, we are committed to offering a comprehensive, competitive and thoughtfully designed total rewards program.
The anticipated salary range for this role is $181,000 - $213,000. The final offer will be determined based on a variety of factors, including role scope, experience and qualifications, education, market benchmarks, internal equity, and geographic location. In addition to base salary, Stoke offers an annual bonus and equity participation.
Our benefits package includes medical, dental and vision insurance; life, long- and short-term disability insurance; paid parental leave; a 401K plan with company match, unlimited vacation time, tuition assistance and participation in our Employee Stock Purchase Program (ESPP).
Medical, dental and vision insurance
Life and disability insurance
Paid parental leave
401(k) with company match
Unlimited vacation
Tuition assistance
Where you'll work
Bedford, MAHybridOpen in Maps (opens in a new tab)
More jobs in Bedford, MAWorking conditions
Travel
This position will require approximately [0%] travel, unless remote then periodic travel to Bedford/ Waltham is expected.
Location(s)
Stoke is located in Bedford, MA, and will be moving to a new location in Waltham, MA by the end of 2026. This position is a hybrid position, or remote, currently based in Bedford and will later be based in Waltham.
From the posting
About Stoke Therapeutics
About Stoke
Stoke Therapeutics (Nasdaq: STOK), is a biotechnology company dedicated to restoring protein expression by harnessing the body’s potential with RNA medicine. Using Stoke’s proprietary TANGO (Targeted Augmentation of Nuclear Gene Output) approach, Stoke is developing antisense oligonucleotides (ASOs) to selectively restore naturally-occurring protein levels. Stoke’s first medicine in development, zorevunersen, has demonstrated the potential for disease modification in patients with Dravet syndrome and is currently being evaluated in a Phase 3 study. Stoke’s initial focus are diseases of the central nervous system and the eye that are caused by a loss of ~50% of normal protein levels (haploinsufficiency). Proof of concept has been demonstrated in other organs, tissues, and systems, supporting broad potential for Stoke’s proprietary approach. Stoke is headquartered in Bedford, Massachusetts. For more information, visit https://www.stoketherapeutics.com/
Culture & Values
At Stoke, we believe that innovation, the ability to successfully advance our ground-breaking science and having fun as a team are enhanced by being together in person, at least periodically. We allow for flexibility in work arrangements that balance individual’s needs and preferences with the needs of our business and our desire to foster a culture of collaboration and innovation.
Our values guide our work to deliver meaningful medicines for people who need them. We are committed to being true to ourselves, to our colleagues, and to the people with severe diseases who are counting on us. We embrace diversity within a unique culture that is defined by our values. Our employee-led Diversity, Inclusion, and Belonging (DIB) Committee underscores the importance of DIB to who we are and what we do.
https://www.stoketherapeutics.com/careers/
For more information, visit https://www.stoketherapeutics.com/.
Equal opportunity, accessibility and legal noticesStoke Therapeutics's statements, word for word
All applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, physical or mental disability or protected veteran status.
Stoke participates in E-Verify.
Job intelligence
The context around this role
Live data · October 15, 2026
Salary intelligence
How the pay compares
This role's midpoint is 15% above the US median for Regulatory CMC roles at this level.
This roleEmployer provided
Manager roles in the US15 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $181,000 | — | $213,000 |
| All US (middle half) | $157,000 | $171,000 | $180,750 |
This role: Stoke Therapeutics's own published range. Comparisons: the base pay employers published on open Regulatory CMC roles at the same level on Regulatory Jobs, October 15, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Regulatory CMC
The general path across 82 open Regulatory CMC roles on Regulatory Jobs, with the titles they carry most. Not Stoke Therapeutics's own promotion track.
Career resources on Regulatory CMC
Skills DNA
What this role leans on
How many of the posting's 20 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Documentation and SOPs6
- Regulatory submissions4
- Collaboration and leadership4
- GMP and compliance2
- Quality systems and risk2
- Lab testing and methods1
- Validation and qualification1
- Data and digital systems1
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
Company hiring pulse
Stoke Therapeutics on Regulatory Jobs
- 4
- Open roles
- 4
- Distinct roles
- 1
- Locations
By discipline
- Regulatory3 75%
- Quality1 25%
By level
- Director2 50%
- VP & Executive1 25%
- Manager1 25%
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Senior Manager, Regulatory Affairs, CMC at Stoke Therapeutics
Open until filled. $181K–$213K a year, employer provided.