Search the 11 jobs at Dyne Therapeutics

The Associate Director, CMC Biologics will lead biologics program execution, manage external CDMOs, and oversee process improvements in a cGMP environment. The role involves cross-team collaboration and communication with stakeholders, alongside document preparation for regulatory submissions.

The Director, Drug Safety & Pharmacovigilance Scientist is responsible for monitoring drug safety, ensuring regulatory compliance, managing safety signals, and leading cross-functional teams at Dyne Therapeutics, focusing on innovative therapeutics for muscle diseases.

The VP Program Team Leader will oversee the development of innovative therapeutics at Dyne, leading cross-functional teams to ensure alignment with program strategy and goals. Responsibilities include managing complex decisions, budgeting, coaching team members, and maintaining communication with stakeholders while advocating for patients' needs in muscle disease therapeutics.

The Associate Director is responsible for strategies and execution of pharmacology data analytics and modeling for drug development at Dyne Therapeutics. This includes PK/PD modeling, collaboration across functions, and supporting regulatory submissions, while managing vendor interactions and leading a modeling workflow.

The Director of Procurement will manage sourcing and contract negotiations, establish a standard process, and improve overall procurement metrics. They will coordinate with internal stakeholders, oversee relationships with managed service providers, draft procurement policies, and provide training.

The Senior Scientist will develop and validate bioanalytical assays for novel therapeutics, utilizing ligand binding techniques in various biological matrices. Responsibilities include assay optimization, performance evaluation, data interpretation, and cross-functional collaboration while ensuring compliance with bioanalytical guidance.

The Associate Director of Biostatistics leads statistical activities for clinical studies, designs innovative trials, prepares statistical plans, and communicates analysis results for regulatory submissions. They collaborate across functions, contribute to protocol and report writing, and oversee outsourced statistical services. The role requires experience in clinical trials and statistical methods, emphasizing effective communication and leadership.

The Associate Director, Statistical Programming leads statistical programming activities for clinical trials, ensuring quality deliverables, collaborating with teams on programming strategies, developing analysis datasets and TLFs, and providing expertise for regulatory submissions. They mentor junior programmers and enhance departmental strategies and standards.

The Senior Director of Quality Management System at Dyne Therapeutics leads the development and implementation of a risk-based QMS framework, ensures quality oversight, and manages internal/external audit programs. This role also involves collaboration across teams, maintaining compliance with standards, and managing budgets and contracts.

The Principal Scientist in Bioinformatics Data Science at Dyne Therapeutics will lead data analytics to accelerate R&D programs. Responsibilities include developing computational methods for analyzing genetic and omics data, employing AI and machine learning techniques, and collaborating with biology and platform development teams to enhance therapeutic opportunities.

The Senior Accountant will be responsible for supporting the finance team with the monthly close process, reconciliations, journal entries, and various finance projects. This role also includes analyzing variances, reviewing GL transactions, ensuring compliance with accounting standards, and assisting with audits and operational support.