Full-time · On-site

Director of Compliance

This is a high-impact leadership role designed for a compliance expert who thrives in the 'pre-launch' phase of a biotech's lifecycle. You will bridge the gap between legal requirements and commercial execution, ensuring Dyne's innovative muscle-targeting therapies reach patients ethically. It is a rare chance to build a department's culture and operational standards from scratch.

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Hiring company

Dyne Therapeutics

Waltham, Massachusetts, United States · Posted 26 April 2026

The role

Overview

This is a high-impact leadership role designed for a compliance expert who thrives in the 'pre-launch' phase of a biotech's lifecycle. You will bridge the gap between legal requirements and commercial execution, ensuring Dyne's innovative muscle-targeting therapies reach patients ethically. It is a rare chance to build a department's culture and operational standards from scratch.

The hiring side

About Dyne Therapeutics

Dyne Therapeutics is a mid-sized employer working in biotechnology, based in Waltham, Massachusetts, United States.

Industry

Biotechnology

Size

Medium

Location

Waltham, Massachusetts, United States

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What they need

Requirements & Skills

Key Responsibilities

  • Design and execute a comprehensive global healthcare compliance program
  • Refresh and establish corporate policies for Commercial, Medical, and Research activities
  • Lead organizational risk assessments to prioritize and mitigate compliance threats
  • Develop risk-based training modules for a diverse employee base
  • Partner with Franchise Counsel to deliver unified legal and compliance advice
  • Act as a champion for the company's core values and culture of integrity

Essential

  • Minimum of 10 years of total professional experience
  • At least 7 years of dedicated healthcare compliance experience
  • Proven experience in the pharmaceutical or biotechnology industry
  • Deep understanding of FDA regulations and healthcare fraud and abuse laws
  • Experience with Value & Access matters and patient support programs
  • Ability to lead confidential and thorough internal investigations
  • Expertise in designing and implementing auditing and monitoring plans

Preferred

  • Prior experience with rare-disease therapeutics
  • Direct experience managing compliance through a first-time product launch
  • Advanced degree in Law (JD) or Business Administration (MBA)

Key Skills

Strategic risk assessmentPolicy development and implementationCross-functional collaborationRegulatory interpretationCurriculum development for compliance trainingData privacy managementEthical leadership

Networking

People to Know

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Perks

Benefits & perks

  • Opportunity to lead a global compliance program
  • Direct impact on rare disease patient communities
  • Collaborative and mission-driven work environment
  • Professional growth within a scaling clinical-stage company

Next step

Apply now

Found via jobs.biospace.com

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