Senior Manager, Clinical Supply
Dyne TherapeuticsAbout the role
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 myotonic dystrophy type 1 (DM1) and Duchenne muscular dystrophy (DMD), and 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 https://www.dyne-tx.com/, and follow us on X, LinkedIn and Facebook.
Role Summary:
The Senior Manager Clinical Supply manages, and monitors activities related to ongoing clinical trial operations and systems to ensure supply continuity. In addition, the role supports readiness of the clinical label and pack set up, global trial distribution network and clinical trial systems for upcoming clinical studies.
The Senior Manager closely interfaces Clinical Operations, Quality, Product Development, Regulatory Affairs, Contract Manufacturing Organization (CMO), Contract Research Operations (CRO’s) and clinical sites to ensure clinical trial supply material is available as required and readiness of the clinical supply network work support the clinical trial strategy. The clinical supply team also provides critical input to set the clinical trial strategy.
This is a full-time position based in Waltham, MA
Primary Responsibilities Include:
Clinical Trial Supply
- Oversee clinical supply operations, including labeling, packaging, distribution, and resupply across global depots
- Manage depot and site inventory in collaboration with Trial Managers; ensure timely IMP and placebo shipments globally
- Coordinate labeling and packaging activities with Clinical CMOs and monitor international shipping and distribution
- Manage exceptions in Quality Systems (deviations, investigations, CAPAs, specifications, and change controls)
- Ensure readiness of labeling, packaging, and distribution networks for future trials
- Align with Supply Planning on demand forecasts, manufacturing outputs, and supply continuity; reconcile inventory and shipments monthly
- Lead development and updates of pharmacy manuals for Phase I–III trials; provide input to clinical strategy and study protocols
- Manage product returns, replacements, and destruction in collaboration with Clinical Operations and Quality
- Identify and implement process improvements; act as SME during regulatory audits
- Represent Clinical Supply on global project teams and collaborate cross-functionally to build capabilities
- Author and maintain SOPs and work instructions for inventory, IRT, labeling, distribution, returns, and destruction
Network Logistics Support
- Coordinate shipments between CMOs, warehouses, 3PLs, test labs, and other nodes
- Support network resupply with internal teams and external partners (couriers, customs brokers, CMOs)
- Ensure compliant, timely shipments including documentation, booking, tracking, and closure
- Troubleshoot logistics issues and implement corrective actions
Education, Experience, and Skills Requirements:
- BS/BA degree (Masters preferred) in life sciences or business major or equivalent required.
- 5+ years of related experi
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