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RhyGaze
RhyGaze
BiotechnologijaFarmacijos produktaiSveikatos priežiūra
„RhyGaze“ yra biotechnologijų įmonė, kurianti genų terapijas, skirtas regėjimui atkurti. Jos veikla orientuota į genetinius ir biologinius akių ligų gydymo metodus, derinant biotechnologijų, sveikatos priežiūros ir farmacijos tyrimus, siekiant sukurti naujus regėjimo praradimo gydymo būdus. Įmonė veikia kaip nedidelė komanda mokslinių atradimų ir regėjimo atkūrimo sankirtoje.
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Darbai įmonėje

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.

CHŠveicarijaHibridinisVisas etatasVadovasPrivaloma Kalba: anglųDirektorius
Google Cloud Platform

Aprašymas

  • 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.

Reikalavimai

  • 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.

Privalumai

  • 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.

Susiję darbai

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