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Stoke Therapeutics

Develops targeted gene upregulation therapies

Vice President - Pharmaceutical & Process Development

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeBedford, MA, USA

About the Job

Requirements

  • A PhD in Chemical Biology, Biomedical Engineering, Chemical Engineering, or a related discipline, with 12+ years of progressive pharmaceutical, biotechnology, or life sciences industry leadership experience spanning formulation, novel delivery technologies, medicinal chemistry, process and analytical development, platform strategy, and organizational leadership.
  • Strong understanding of and experience with developability assessment criteria and global chemistry, manufacturing, and controls (CMC) and regulatory guidance and expectations for development and commercialization of complex modalities, including oligonucleotides (ASO, siRNA) and nucleic acid therapeutics.
  • A distinguished record of scientific innovation, reflected through publications, patents, investigational new drug applications (INDs), clinical trial applications (CTAs), new drug applications (NDAs), biologics license applications (BLAs), and advancement of therapeutics with novel mechanisms of action and/or delivery into preclinical and clinical development.
  • Demonstrated ability to leverage internal capabilities, external innovation, and strategic collaborations to operationalize strategic plans and advance platform technologies from discovery through clinical development.
  • A proven track record building and leading high-performing integrated teams, developing talent, and balancing enterprise priorities across efficiency, risk, and innovation.
  • A proven track record of innovation, strategic thinking, problem-solving, cross-functional collaboration, data-driven decision-making, and organizational skills.
  • Ability to build and sustain an inclusive, collaborative culture that supports innovation and continuous improvement.
  • Exceptional verbal and written communication skills, with the ability to distill technically complex topics for varied audiences, present recommendations, and drive alignment with senior leadership and cross-functional stakeholders.
  • Ability to navigate and influence within a complex matrix organization.

Responsibilities

  • Define and execute an enterprise-level strategic roadmap for oligonucleotide-based therapeutics, spanning nucleotide medicinal chemistry, process and analytical sciences, delivery strategy, and formulation innovation.
  • Advance platform innovation within an R&D environment to broaden the reach, differentiation, and therapeutic impact of oligonucleotides in regulating disease-relevant gene expression.
  • Identify, assess, and integrate novel technologies that extend the impact of TANGO and other nucleic acid approaches by improving target presentation and engagement across disease-relevant tissues and cell types.
  • Provide senior technical leadership and fluency across ASO, siRNA, and PMO technologies, including chemistry, process and analytical sciences, delivery strategy, and formulation approaches.
  • Build, lead, and scale high-performing scientific teams responsible for nucleic acid chemistries, bioconjugates, delivery systems, process development, analytical characterization, biological validation, and technical implementation.
  • Apply scientific insight, strategic judgment, and disciplined governance to evaluate therapeutic concepts and platform technologies based on potential impact, differentiation, and product or technology risk.
  • Partner with R&D and program leadership to shape early-stage therapeutic concepts, inform strategic direction and resourcing decisions, and support selection and advancement of pipeline candidates.
  • Establish and steward external partnerships and collaborations that expand Stoke’s technological capabilities in alignment with the organization’s mission and strategic priorities.
  • Represent platform capabilities and technologies with credibility and influence among internal stakeholders, external scientific leaders, partners, and collaborators.

About the Company

Stoke Therapeutics

Develops targeted gene upregulation therapies

Stoke Therapeutics develops therapies for severe genetic diseases caused by loss of function in a single gene, aiming to restore missing proteins by upregulating protein expression. Its main product approach relies on the TANGO (Targeted Augmentation of Nuclear Gene Output) platform, which delivers precise, durable, and controllable upregulation of gene expression across a range of tissues to re-create the missing protein. Compared with many biotech firms, Stoke centers on upregulating endogenous gene output rather than replacing genes or adding new ones, and focuses on disease-modifying treatments for rare disorders with unmet medical needs. Revenue comes from partnerships, licensing agreements, and, ultimately, commercialization of its therapies. The company’s goal is to provide targeted, durable treatments that address the underlying genetic deficiency and improve outcomes for patients with limited options.

Company size
201-500
Company stage
IPO
Headquarters
Bedford, TX
Founded
2014

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