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Director Regulatory Affairs

Dyne Therapeutics

🇺🇸 United States
Base Salary
40k-80k USD (est.)
Dyne Therapeutics

Job Description

Role Summary:

The Director, Regulatory Affairs helps drive forward our regulatory strategy and operational activities related to Dyne’s muscle disease programs. The person in this role must thrive working in a fast-paced environment where flexibility, accountability and fearless innovation are key. Additionally, this individual must have excellent interpersonal skills, ability to develop important relationships with key stakeholders, good conflict management and negotiation skills, ability to analyze complex issues to develop relevant and realistic regulatory and strategies. A shared passion for Dyne’s mission to bring transformative therapies to people living with serious muscle diseases is a must.

This role is based in Waltham, MA without the possibility of being a remote role. Applicants must be able to relocate to the area. Primary Responsibilities Include:

  • Interact with other departments to develop regulatory strategy and submission plans for quality and timely filings

  • As a member of program teams, provide global regulatory guidance regarding requirements for clinical development and registration of pharmaceuticals

  • Oversee preparation, review, and submission of regulatory documents maintaining compliance with regulatory requirements.

  • Manage timelines and preparation of meeting requests and briefing documents

  • Author/edit documents to support regulatory submissions

  • Compile, review, approve and submit clinical trial and marketing registration applications, amendments, and supplements

  • Manage and ensure compliance with all reporting requirements, including annual and periodic reports

  • Support the organization with health authority meetings

  • Provide strategic guidance for and author applications related to expedited programs/designations for rare muscle disease (e.g. Fast Track, Orphan Drug Designation, etc)

  • Manage staff and vendors as needed to support regulatory activities

  • Assist with SOP generation

  • Perform other duties as required, interfacing with other departments, CROs and external vendors as needed

Education, Knowledge & Skill Requirements

  • Minimum of a bachelor’s degree in life science or related discipline is required

  • Minimum of 8-10 years of experience in regulatory strategy in a clinical-stage biotechnology company

  • Strong experience with CTD format and content regulatory filings

  • Experience and knowledge in the preparation of major regulatory submissions and supportive amendments or supplements

  • Experience in Health Authority Meetings

  • Knowledge of EU and international regulations related to the clinical, nonclinical, and CMC development a plus

  • Ability to work independently to manage multiple projects in a fast-paced environment

  • Ability to effectively collaborate in a dynamic, cross-functional matrix environment to drive meeting each program’s critical regulatory milestones

  • Effectively communicate the regulatory strategy, risks, mitigations, and overall plans to Project Teams and senior management

  • Outstanding communication skills (verbal and written), regulatory writing skills and willingness to share knowledge and lessons learned


Salary and compensation

                                                                                                        No salary data published by company so we estimated salary based on similar jobs related to Senior, Marketing and Non Tech jobs that are similar:

                                                                                                                                                             $40,000 — $80,000/year



                                                💰 401(k)

🌎 Distributed team

⏰ Async

🤓 Vision insurance

🦷 Dental insurance

🚑 Medical insurance

🏖 Unlimited vacation

🏖 Paid time off

📆 4 day workweek

💰 401k matching

🏔 Company retreats

🏬 Coworking budget

📚 Learning budget

💪 Free gym membership

🧘 Mental wellness budget

🖥 Home office budget

🥧 Pay in crypto

🥸 Pseudonymous

💰 Profit sharing

💰 Equity compensation

⬜️ No whiteboard interview

👀 No monitoring system

🚫 No politics at work

🎅 We hire old (and young)


Waltham, Massachusetts, United States

Advice from our career coach

Are you ready to take on the role of Director, Regulatory Affairs at Dyne? In this fast-paced position, you'll drive our regulatory strategy and operational activities for our muscle disease programs. We're looking for someone who thrives on flexibility, accountability, and fearless innovation. Excellent interpersonal skills, the ability to develop relationships with key stakeholders, and strong conflict management and negotiation skills are a must. If you have a passion for bringing transformative therapies to people with serious muscle diseases, then this is the job for you. Based in Waltham, MA, this is not a remote role, so you must be able to relocate. Join us in making a difference!

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About the job

Feb 8, 2024


40k-80k USD (est.)

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