Dyne Therapeutics

Senior Director, Managed Access Programs

Dyne Therapeutics$233K — $285K *
Pharmaceuticals & Biotech
11 - 15 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree with rare disease experience in biotech/pharmaceutical; neuromuscular experience preferred
  • 15+ years in Medical Affairs with global Managed Access Programs experience
  • Proven leadership in Managed Access Program development and execution
  • Excellent communication skills with KOLs and cross-functional teams
  • Experience with AI-supported methodologies
  • In-depth understanding of healthcare regulations and access environments
  • Flexibility to adapt to changing customer needs and a matrix environment

Responsibilities

  • Lead the strategic direction and execution of managed access programs
  • Build and oversee infrastructure for program implementation
  • Oversee vendor management for program administration
  • Foster collaboration and innovation among teams to address patient access challenges
  • Design comprehensive policies that ensure regulatory compliance and patient access
  • Analyze program performance to refine strategies and enhance effectiveness
  • Cultivate relationships with external stakeholders to promote managed access initiatives

Benefits

  • Comprehensive training programs for internal teams
  • Opportunities for professional development and growth
  • Travel opportunities to meet with stakeholders and attend conferences
  • Collaborative and innovative work environment
  • Commitment to ethical standards and patient access improvement
Full Job Description
Role Summary:

The Senior Director of Managed Access Programs (MAPs) leads the strategic direction and operational execution of managed access initiatives across the organization. This role is crucial in designing, implementing, and managing global programs that ensure patient access to our innovative therapeutics. This role develops policies and procedures that support equitable access while adhering to regulatory standards. This position collaborates closely with internal teams, including market access, HEOR, medical affairs, commercial, clinical, regulatory, supply chain, legal, and compliance to align MAP initiatives with the overall goals of the organization.

In addition, the person in this role partners with cross-functional teams to build and maintain strong relationships with key external stakeholders, to promote understanding and support for managed access programs. With a focus on data-driven decision-making, this role analyzes program performance, adjusting strategies as needed to maximize impact. By providing training and support to internal teams, this role ensures effective implementation of MAPs initiatives across the organization. Ultimately, this role plays a vital part in navigating complex access environments and improving health outcomes for patients.

This role is based in Waltham, MA.

Primary Responsibilities Include:
  • Provide visionary leadership in the development and execution of managed access programs, ensuring that strategies align with Dyne Therapeutics' mission and objectives
  • Build and oversee infrastructure necessary to implement managed access programs
  • Oversee vendor responsible for program administration
  • Foster a culture of collaboration and innovation within organization, guiding teams in effectively addressing patient needs and access challenges
  • Design and implement comprehensive managed access policies and procedures that promote patient access to innovative therapies, with an emphasis on maintaining compliance with evolving regulatory requirements
  • Utilize best practices and learnings from the field to continuously refine and enhance program frameworks
  • Lead cross-functional teams, including Clinical Development, Regulatory Affairs, and Commercial, to ensure successful integration of managed access strategies across all stages of product development and commercialization
  • Act as a key liaison, facilitating clear communication and alignment on priorities and objectives
  • Establish and cultivate strong relationships with a diverse range of external stakeholders, including healthcare professionals, patient advocacy organizations, and regulatory bodies as appropriate
  • Represent Dyne Therapeutics at conferences, meetings, and roundtable discussions, effectively advocating for managed access initiatives and fostering stakeholder trust and support
  • Partner with HEOR, Market Access, Medical Affairs, and Clinical Development to implement data collection and analytics methodologies to assess program efficacy, patient outcomes, and potential access barriers
  • Generate and present comprehensive reports to senior leadership and external stakeholders, offering actionable insights and recommendations for program improvement
  • Develop and deliver targeted training programs and resources for internal teams regarding managed access processes, regulatory compliance, and best practices
  • Ensure team is well-equipped to effectively engage with external partners and navigate complex access scenarios
  • Continuously monitor and analyze industry trends, regulatory changes, and market dynamics that impact managed access programs
  • Provide strategic recommendations to adapt and evolve Dyne Therapeutics' approach to access challenges in response to the shifting landscape
  • Oversee the financial aspects of managed access programs, including budget planning, forecasting, and resource allocation
  • Ensure that objectives are met while maximizing the impact of programs on patient access initiatives
  • Foster a culture of excellence by encouraging feedback and facilitating continuous improvement within managed access programs
  • Utilize lessons learned from program implementation and stakeholder interactions to drive innovation and enhance the overall effectiveness of initiatives

Education and Skills Requirements:
  • Bachelor's degree with rare disease experience in the biotech and/or pharmaceutical industry; neuromuscular experience preferred
  • 15+ years of relevant experience in Medical Affairs and experience in leading global Managed Access Programs within the pharmaceutical/biotech industry; clinical operations experience also desirable
  • Proven ability to lead global Managed Access Program development and implementation
  • Excellent communication and relationship-building skills with KOLs and cross-functional teams
  • Experienced in AI supported way of working
  • Ability to interpret and communicate complex scientific data to diverse audiences
  • Must be willing to travel up to 30%, inclusive of overnight and occasional weekends, to meet with customers, internal stakeholders and attend relevant conferences
  • In-depth understanding of healthcare regulations, access environments, and the pharmaceutical industry landscape
  • Familiarity with rare diseases and innovative therapies is highly desirable
  • Strong leadership and interpersonal skills, with the ability to influence and drive cross-functional collaboration
  • Excellent analytical and problem-solving capabilities.
  • Exceptional verbal and written communication skills, with the ability to convey complex information clearly to diverse audiences (written, verbal and presentation)
  • Proven track record of developing and executing successful managed access strategies that improve patient access and outcomes
  • Excellent team player
  • Strong decision maker
  • Ability to work in a matrix environment
  • Ability to work independently as a hands-on manager, proactively contribute as a resource when necessary
  • Flexibility to adapt and meet the changing/growing needs of our customers
  • High level of integrity, compliance, ethics, and transparency
  • Positive team member who embodies Dyne's Core Values
  • Excitement about Dyne's vision and mission

#LI-Onsite

MA Pay Range

$233,000-$285,000 USD

The pay range reflects the base pay range Dyne reasonably expects to pay for this role at the time of posting. Individual compensation depends on factors such as education, experience, job-related knowledge, and demonstrated skills.

The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements. Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.

About Dyne Therapeutics

Dyne Therapeutics is a biotechnology company that is focused on developing therapies for patients with genetically driven muscle diseases. The company is developing a platform that is designed to deliver nucleic acids to muscle tissue. Dyne's lead product candidate is DYN101, which is a treatment for patients with myotonic dystrophy type 1 (DM1). DM1 is a genetic disorder that affects the muscles and other body systems. DYN101 is designed to reduce the levels of toxic RNA that are produced by the mutated gene that causes DM1. The company was founded in 2018 and is headquartered in Cambridge, Massachusetts.
Learn more about Dyne Therapeutics
Size
70 employees
Market Cap
$633.4 million
Industry
NASDAQ

Similar Jobs

More Jobs at Dyne Therapeutics

More Pharmaceuticals & Biotech Jobs

Find similar Senior Director, Managed Access Programs jobs: