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Stoke Therapeutics

Develops targeted gene upregulation therapies

Vice President - Clinical Development, Ophthalmology

Biology & BiotechConfirmed live in the last 24 hours
Full-timeBedford, MA, USA

About the Job

Requirements

  • An M.D. or M.D./Ph.D. degree is required.
  • Board certification in Ophthalmology is strongly preferred.
  • At least 12–15 years of biopharmaceutical industry experience, including substantial clinical development leadership responsibilities.
  • Demonstrated experience leading clinical development programs in ophthalmology.
  • Experience authoring or overseeing clinical development plans, protocols, investigator brochures, and regulatory submissions.
  • Strong understanding of global regulatory requirements and interactions with health authorities.
  • Proven leadership experience managing cross-functional teams and influencing executive decision-making.
  • Excellent communication, presentation, and stakeholder engagement skills.

Responsibilities

  • Lead clinical development strategy for ophthalmology programs from IND-enabling activities through registration and life-cycle management.
  • Serve as the medical and scientific leader for assigned development programs, ensuring alignment with corporate objectives and portfolio strategy.
  • Design and oversee Phase 1–3 clinical trials, including protocol development, endpoint selection, statistical considerations, and clinical study interpretation.
  • Provide strategic leadership for regulatory interactions with the FDA, EMA, PMDA, and other global health authorities.
  • Drive development plans that maximize the probability of technical, clinical, regulatory, and commercial success.
  • Partner with Clinical Operations, Biostatistics, Regulatory Affairs, Translational Medicine, Medical Affairs, and Commercial teams to ensure successful program execution.
  • Serve as the program representative on the Ophthalmology Program Team.
  • Chair clinical development teams and governance committees as appropriate.
  • Build and maintain relationships with key opinion leaders, investigators, patient advocacy groups, and strategic partners.
  • Support business development activities.
  • Recruit, develop, and mentor clinical scientists and physician leaders.
  • Foster a culture of scientific excellence, collaboration, accountability, and patient focus.
  • Establish best practices for clinical development and medical governance across the organization.

Desired Qualifications

  • Direct experience developing therapies for rare ophthalmic diseases and inherited retinal disorders.
  • Experience with gene therapy, gene editing, RNA-based therapies, or other advanced therapeutic modalities.
  • Track record of advancing programs through pivotal studies and regulatory approval.
  • Established relationships with leading ophthalmology investigators, retinal specialists, and academic centers.
  • Prior experience in a biotechnology company environment.

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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