Stoke Therapeutics, Inc.

Associate Director, Publications

Stoke Therapeutics, Inc.$193K — $219K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Advanced degree in relevant scientific or clinical fields preferred (MD, DO, PA, NP, PhD, PharmD, MS)
  • 7+ years of publication writing experience in a pharmaceutical/biotech or medical communication agency
  • 5+ years managing publication execution from concept to submission
  • Expertise in publication review and approval processes
  • Experience with clinical trial data analysis
  • Familiarity with publication review systems preferred (e.g., Datavision, Komodo)
  • Rare disease therapy experience preferred

Responsibilities

  • Write and edit scientific publications including abstracts and journal articles
  • Lead review and submission processes for publications
  • Coordinate development and approval of publications with external authors
  • Facilitate monthly publication team meetings for strategic alignment
  • Ensure compliance with publication guidelines and company policies
  • Manage external agency partners for quality and timelines
  • Participate in annual cross-functional publication planning

Benefits

  • Medical, dental, and vision insurance
  • Life, long- and short-term disability insurance
  • Paid parental leave
  • 401K plan with company match
  • Unlimited vacation time
  • Tuition assistance
  • Employee Stock Purchase Program (ESPP)
Full Job Description
Position Purpose:

The Associate Director, Publications will be responsible for leading the execution of the scientific publication plan, including the development and submission of manuscripts, abstracts, oral presentations, and posters. This individual will serve as the central point of coordination across authors and internal functions, ensuring consistency, quality, and scientific rigor across all publications while maintaining adherence to publication standards and regulations. In addition, this role will partner with Medical Affairs colleagues to contribute to the development of educational materials. This work is essential for amplifying the visibility of our data, shaping external scientific dialogue, and reinforcing our leadership in the field.

This position will report into the Senior Director, Publications.

Key Responsibilities:
  • Write and/or edit medical publications, including abstracts, conference presentations, journal articles, and other educational medical communications materials (e.g., slide decks, training modules, scientific platforms, etc.).
  • Lead the process for review, approval, and submission/presentation of publications.
  • Coordinate with external authors for the development, review, and approval of publications.
  • Lead monthly publication team meetings to ensure cross-functional strategic alignment on publication projects and discuss updates to and preparation for the annual plan.
  • Ensure compliance with ICMJE/GPP and company policies and procedures for publications, including advances and guideline updates.
  • Manage external agency partners, as needed, to ensure quality and timelines of publications are met.
  • Participate in and/or manage aspects of annual cross-functional publication planning.
  • Participate in or lead other cross-functional communication projects, as needed, to support innovation in external engagement and scientific dissemination.

Required Skills & Experience:
  • Advanced degree in relevant scientific or clinical fields strongly preferred (MD, DO, PA, NP, PhD, PharmD, MS) preferred
  • Minimum of 7 years of experience in writing about clinical data for presentation and journal article publication within a pharmaceutical/biotech company or scientific publication/medical communication agency
  • Minimum 5 years of experience managing the execution of publications from concept initiation to submission/publication, including addressing peer reviewer comments and/or revising for resubmission/encoring
  • Expert understanding of all the internal and external review and approval steps in the publication process
  • Experience managing and tracking multiple complex projects in parallel, structuring the actions of stakeholders/authors toward shared outcomes
  • Understanding of clinical trial conduct and analysis of clinical trial data
  • Depth of knowledge of ICMJE/GPP guidelines
  • Familiarity with publications review systems (e.g., Datavision, Komodo) is preferred
  • Rare disease therapy area experience is preferred
  • Analytical thinker with excellent problem-solving skills and the ability to adapt to changing priorities and deadlines
  • Ability to develop positive collaborative relationships with external experts in the relevant therapeutic area
  • Experience working with all levels of management and consulting with key business stakeholders
  • Ability to work independently and collaboratively, as required, in a fast-paced start-up environment
  • Strong team player who has a customer- and solution-oriented approach

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 open to remote or hybrid work arrangements.

Travel:

This position will require approximately 15% travel.

Compensation & Benefits:

At Stoke Therapeutics, we are committed to offering a comprehensive, competitive and thoughtfully designed total rewards program.

The anticipated salary range for this role is $193,000 - $219,000. 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).

About Stoke Therapeutics, Inc.

Stoke Therapeutics is a biotechnology company that is focused on developing treatments for severe genetic diseases. The company's approach is to use antisense oligonucleotides to increase gene expression levels in order to treat the underlying genetic cause of the disease. Stoke's lead program is focused on Dravet syndrome, a severe form of epilepsy that is caused by mutations in the SCN1A gene. The company is also developing programs for other genetic diseases, including genetic forms of ALS and Huntington's disease.
Learn more about Stoke Therapeutics, Inc.
Size
102 employees
Market Cap
$328.4 million
Industry
Net Income
-$52.2 million
NASDAQ

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