Senior Director, Program Management
Company: Dyne Therapeutics
Location: Waltham
Posted on: March 19, 2026
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Job Description:
Company Overview: Dyne Therapeutics is focused on delivering
functional improvement for people living with genetically driven
neuromuscular diseases. We are developing therapeutics that target
muscle and the central nervous system (CNS) to address the root
cause of disease. The company is advancing clinical programs for
Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1
(DM1) as well as a preclinical programs for facioscapulohumeral
muscular dystrophy (FSHD) and Pompe disease. At Dyne, we are on a
mission to deliver functional improvement for individuals, families
and communities. Learn more at https://www.dyne-tx.com/ , and
follow us on X , LinkedIn and Facebook . Role Summary: The Senior
Director, Program Management (PM) is a critical role within the
cross-functional development team responsible for facilitating and
driving execution across the wide spectrum of activities required
for successful development of one or more molecules. The PM
partners closely with the Program Team Leader (PTL) and functional
subject matter experts to ensure that plans are in place with
appropriate detail and risk awareness to assure successful
achievement of the goals of the development team. The PM ensures
integration of these detailed functional plans into a holistic,
cohesive, and comprehensive program plan that achieves the
strategic goals of the development program. Given the inherent
uncertainty associated with drug development in rare disorders, the
PM maintains an agile mindset in order to effectively incorporate
and react to emerging data and course correct as conditions
dictate. Working in close partnership with the PTL, the PM
effectively frames and facilitates discussions with team members
and external experts to elicit clear recommendations and decisions
by fully engaging with team members to consider multiple options
with a focus on impact on quality, time, and cost. Their influence
and engagement skills allow them to work with a highly motivated
team and manage stakeholders at all levels of the company. This
role is based in Waltham, MA without the possibility of being a
remote role. Primary Responsibilities Include: Lead the operations
of one or more high performing cross-functional teams, with focus
on both the “what”, such as priorities, goal achievement, and
resources, and the “how” of maintaining a challenging,
collaborative, and sustainable team environment Partner with the
PTL to identify short, medium, and long-term team priorities and
propose path to address Drive execution of the established and
aligned Program vision and strategy for bringing a life-changing
medicine to patients in need Facilitate creation & maintenance of
core program strategy documents including Target Product Profile
(TPP), Clinical Development Plan, Regulatory Strategy, and Supply
Strategy in collaboration with cross-functional representatives
Ensure that non-clinical, clinical, regulatory, and
commercialization strategies and plans are aligned with the TPP and
the overall Program Strategy Inspire development of an efficient
plan to achieve development and commercialization strategy,
optimizing for quality, speed and cost Ensure that program
decisions are made in a timely, clear and efficient manner through
interactions with the PTL, Program Team members, governance forums
and other key stakeholders Accountable for creation and maintenance
of detailed cross-functional plans and effective visual summaries
thereof to instill awareness, build accountability and facilitate
achievement Maintain clear and open communication with Program
Team, Dyne Senior Leadership, and other stakeholders regarding
program status, priorities, risks and needs, and facilitate
appropriate strategic decision-making Partner with Head of Program
Management to evolve Program Management discipline to meet needs of
a growing organization that intends to launch a portfolio of
disease products Keep abreast of emerging developments regarding
research and development in the fields of muscle diseases and
oligonucleotide drug discovery and development Foster a culture of
collaboration, innovation, discovery, and cutting-edge research
culture focused on scientific excellence, open communication, and
continual improvement Education and Skills Requirements: Proven and
respected team member with: Bachelor’s degree in science or related
field; Advanced degree in a scientific discipline or MBA preferred
15 years of relevant experience in biotech/pharmaceutical industry
in positions of increasing responsibility in drug development
Experience with late-stage clinical development and commercial
stage programs required Experience with neuromuscular diseases a
plus Exceptional communication skills (verbal, written,
presentation) and ability to communicate with across a broad group
of stakeholders and teams Proficient with Microsoft Office 365
applications, Smartsheet and other PM management workspace
collaboration tools Expert at cross-functional teamwork and
influencing without direct authority Demonstrated experience in
working with highly effective teams and guiding teams and
organizations in making complex and high-stakes data-driven
decisions Passionate about developing and commercializing
life-transforming therapies for patients with severe and
life-threatening diseases Adept at operating in cross-functional
matrix teams, developing effective relationships based on mutual
trust and effective communication and thrives in a fast-paced,
patient-focused environment Proven ability to establish and
maintain credible and trust-based relationships Outstanding sense
of urgency and ability to help pace the team’s work in highly
competitive environment Orientation towards collective achievement
and team credit, combined with individual sense of responsibility
and accountability for teamwork and product Comfort with ambiguity
and ability to provide steadiness and consistency in environment of
shifting priorities Ability to lead without authority through
complex and ambitious projects in a cross-functional team
environment and high-pressure circumstances Comfortable in a
results-driven, highly accountable environment where you can make a
clear impact Team player who listens effectively and invites
response and discussion A collaborator who communicates in an open,
clear, complete, timely and consistent manner 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. 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.
Keywords: Dyne Therapeutics, North Attleborough , Senior Director, Program Management, Manufacturing , Waltham, Massachusetts