Director, Clinical Operations Program Lead

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 and follow us on X LinkedInand Facebook.

Company Overview:

Dyne Therapeutics is a clinical-stage muscle disease company focused on advancing innovative life-transforming therapeutics for people living with genetically driven its proprietary FORCE platform Dyne is developing modern oligonucleotide therapeutics that are designed toovercome limitations in delivery to muscle has a broad pipeline for serious muscle diseases including clinical programs for myotonicdystrophy type 1 (DM1) and Duchenne muscular dystrophy (DMD) and a preclinical program for facioscapulohumeral muscular dystrophy (FSHD). For more information please visit and follow us on XLinkedInandFacebook.

Role Summary:

The Clinical Operations (Program) Lead is the clinical operations functional representative at the Program team is responsible for developing and leading the strategy planning oversight implementation and delivery of program and study level clinical operations deliverables as outlined in the clinical development plan (CDP).

This individual is responsible for providing advanced functional and technical expertise and insights from both a strategic (decision points risk) and operational (timeline scenarios feasibility & financials) perspective to meaningfully contribute and make recommendations to the integrated development plan (IDP) and other key plans such as the CDP necessary to advance Dynes clinical programs. This individual develops and oversees implementation of program clinical operational strategy ensuring appropriate considerations that include but are not limited to technical vendor quality site/ Investigator geographical and patient centric considerations for the Programs lifecycle. This individual may be responsible for one highly complex or multiple medium complexity clinical programs.

This role is expected to require up to 20% travel including international travel.

This role is based in Waltham MA.

Primary Responsibilities Include:

• Leads the development and ongoing refinement of Program level study timelines and scenariosin order to contribute to the CDP IDP and other high-level strategic plans
• Provide rigorous objective information (operational status and updates) to the Program team and as necessary Dyne senior leadership to help support strategic project decisions.
• Takes overall accountability for operational delivery of the clinical studies within a Program and provide appropriate oversight to ensure a high quality ethical cost efficient way to meet timelines and patient recruitment goals.
• Actively participates in Program team and other applicable sub-team meetings collaborating and integrating with other functions within research and development medical and commercial in order to deliver on the CDP/IDP.
• Responsible for the development and execution of a Program strategic clinical operations plan taking into account the therapeutic area and underlying science and opportunities for innovation and operational consistency as well as the future clinical regulatory and commercial development plan for the molecule. Proactively integrates stage-appropriate needs into the operational strategy.
• Oversees mentors and works collaboratively with Clinical Study Lead(s) and other clinical operations and supportive roles within the Program (clinical trial coordinators quality representative vendor managers etc.)
• Overall accountability overseeing and driving CRO and other vendor relationships to ensure execution of clinical studies within the Program within timelines budget and with quality
• Participates in departmental and cross functional risk assessment technology development and process improvement initiatives including SOP development review and maintenance.
• Participate/lead in site engagement programs to help build relationships with key opinion leaders investigators and clinical site staff to support the clinical study activities and delivery
• Engage with patient advocacy groups to help build patient-focused clinical operations strategies methods and tools for use in the clinical studies
• Create and implement risk assessment and mitigation plans performing regular reviews to continually assess for changes
• Attend seminars congresses advocacy meetings Investigator meetings Program and sub-team meetings educational conferences/training sessions
• Provide management training oversight coaching mentoring and development to one or more direct reports

Education and Skills Requirements:

• Undergraduate degree in a scientific or health related discipline. Advanced scientific or business degree or equivalent experience desirable.
• 10years experience in drug development clinical research and operational strategy experience including responsibility ensuring studies and programs are executed to quality timelines and budget (at least part of this time in a Biotech/Pharma environment is preferred)
• Demonstration of project/program management skills including risk assessment timeline and budget management and contingency planning
• Demonstration of effective team leadership of matrix teams. Excellent communication management and organizational skills along with problem solving conflict resolution and team building skills
• Experienced in identifying and leveraging relevant data and information to develop well-conceived and executable timelines
• Experience across several complex therapeutic areas; neuromuscular or muscle disease experience preferred. Experience with rare disease and/or pediatric trials also preferred
• Scientifically and clinically agile proven ability to learn and apply relevant disease information into strategic operational planning and delivery
• Deep operational expertise. Experience planning and delivering global clinical programs and studies
• Independently motivated detail oriented and good problem-solving ability (think outside of the box mentality)
• Experience in participating or facilitating the development of Clinical Development Plans (CDPs) with multiple functions strongly desired
• Excellent organizational skills with an ability to embrace change and multi-task in an extremely fast-paced environment
• Enjoys building relationships with KOLs and site personnel with a willingness to travel to establish and build relationships
• Experience with engaging and working with Patient Advocacy groups beneficial
• Experience with hiring managing mentoring and/or developing direct reports preferred

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.