Director, Regulatory Affairs

Company Overview: Dyne Therapeutics is focused on discovering and advancing innovative life-transforming therapeutics for people living with genetically driven neuromuscular diseases. Leveraging the modularity of its FORCE platform, Dyne is developing targeted therapeutics that are designed to overcome limitations in delivery to muscle tissue and the central nervous system (CNS). Dyne has a broad pipeline for neuromuscular diseases, including clinical programs for myotonic dystrophy type 1 (DM1) and Duchenne muscular dystrophy (DMD) and preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. 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 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 Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.

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