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Clinical Development Director

RhyGaze AG·Basel, Switzerland·03.06.2026

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Festanstellung80–100%
Required language
English professional
Job written in
English
Location
Basel, Switzerland
Work type
On-site

 

RhyGaze is a growing biotech company focused on developing innovative therapies for serious eye diseases. The Clinical Development Director will play a crucial role in advancing the company's cutting-edge pipeline, particularly in the field of gene therapy. The main responsibilities include leading and supporting clinical development activities, contributing to clinical strategy and study design, and preparing and reviewing key clinical and regulatory documents. The role involves working closely with cross-functional teams, CROs, investigators, and advisors to drive programs forward. Additionally, the director will support regulatory interactions and stay current on advances in ophthalmology and gene therapy to guide program strategy. To excel in this role, candidates must have an advanced scientific or medical degree, such as an MD, PharmD, PhD, or equivalent experience. They need at least five years of clinical development experience in the biotech or pharma industry, with a strong focus on ophthalmology and gene therapy. Specific experience in retina treatments is required, while glaucoma experience is preferred but not mandatory. Nice-to-have skills include a strong understanding of clinical trial design and GCP guidelines, as well as excellent communication, leadership, and collaboration skills. The role is based in Basel, Switzerland, with a requirement to be onsite three days a week. The working language is English, and candidates must have strong written and spoken English skills. Additionally, candidates need to hold a Swiss working permit or be an EU citizen eligible to work in Switzerland. What the role asks for: - Advanced scientific or medical degree (MD, PharmD, PhD, or equivalent experience). - 5+ years of clinical development experience in biotech or pharma. - Ophthalmology experience. - Gene therapy experience. - Retina experience. - Experience preparing and reviewing a broad range of clinical and regulatory documents. - Strong understanding of clinical trial design and GCP guidelines. - Strong written and spoken English skills.

 

 

 

 

 

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