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RhyGaze
RhyGaze
BiotechnologyHealthcarePharmaceuticals
RhyGaze is a biotechnology company developing gene therapies aimed at restoring vision. Its work focuses on genetic and biologic approaches for ocular diseases, bringing together biotechnology, healthcare, and pharmaceutical research in pursuit of new treatments for vision loss. The company operates as a small team working at the intersection of scientific discovery and vision restoration.
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Clinical Development Director, Ophthalmology Gene Therapy

Lead RhyGaze’s clinical development strategy for gene therapies targeting serious eye diseases. The role spans trial design, regulatory planning, and cross-functional program leadership.

CHSwitzerlandHybridFull-timeLeadEnglish RequiredDirector
Google Cloud Platform

Description

  • Guide clinical development across ophthalmology gene therapy programs for anterior and posterior segment diseases.
  • Shape clinical strategy, design studies, and oversee clinical trial execution.
  • Draft and review protocols, investigator brochures, clinical study reports, and regulatory submissions.
  • Advise on patient safety, data review, and overall study conduct.
  • Coordinate with internal teams, CROs, investigators, and advisors to advance programs.
  • Support regulatory discussions and contribute to development plans and milestones.
  • Track advances in ophthalmology and gene therapy to inform program strategy.
  • Report to the Vice President of Clinical Development.
  • Set strategic direction for development plans, study design, endpoint selection, regulatory strategy, and key program milestones.

Requirements

  • An advanced scientific or medical degree (MD, PharmD, PhD, or equivalent experience) is preferred.
  • At least five years of clinical development experience in biotechnology or pharmaceuticals.
  • Ophthalmology experience is required.
  • Gene therapy experience is required.
  • Retina experience is required.
  • Glaucoma experience is preferred but not required.
  • Experience preparing and reviewing a range of clinical and regulatory documents.
  • Strong knowledge of clinical trial design and Good Clinical Practice (GCP) guidelines.
  • Excellent communication, leadership, and collaboration skills.
  • Demonstrated ability to deliver outcomes in collaboration with internal teams and external vendors.
  • Comfort working hands-on in a fast-moving biotechnology environment.
  • Strong spoken and written English.
  • A Swiss work permit or EU citizenship with eligibility to work in Switzerland.

Benefits

  • Help develop new therapies for patients with serious, vision-threatening diseases.
  • Work with an experienced, committed team advancing ophthalmology innovation.
  • Make a meaningful contribution at a growing biotechnology company.
  • Join a collaborative, entrepreneurial culture guided by science and innovation.

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