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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical development within ophthalmology, particularly in gene therapy, with a strong focus on study design, regulatory strategy, and cross-functional collaboration. Proven ability to lead clinical programs and ensure compliance with GCP guidelines while effectively communicating with diverse stakeholders.
Highest-signal resume keywords
Clinical Development ExperienceOphthalmology ExpertiseGene Therapy KnowledgeClinical Trial DesignRegulatory Document Preparation
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical DevelopmentGene TherapyOphthalmologyClinical Trial DesignGCP GuidelinesRegulatory SubmissionsData ReviewStudy ExecutionProtocol PreparationClinical Study Reports
Soft Skills
LeadershipCollaborationCommunicationStrategic InsightProblem-Solving
Certifications & Qualifications
Advanced Scientific Degree (MD, PharmD, PhD)
Industry Keywords
BiotechPharmaRetinaGlaucomaClinical StrategyCross-Functional TeamsCROsPatient SafetyDynamic EnvironmentSwiss Working Permit
About the role
Key responsibilities & impact- Lead and support clinical development activities across ophthalmology programs, focusing on gene therapy programs targeting both anterior and posterior segment eye diseases
- Contribute to clinical strategy, study design, and execution of clinical trials
- Prepare and review key clinical and regulatory documents, including protocols, investigator brochures, clinical study reports, and regulatory submissions
- Provide clinical insight into patient safety, data review, and overall study conduct
- Work closely with cross-functional teams, CROs, investigators, and advisors to drive programs forward
- Support regulatory interactions and contribute to development plans and milestones
- Stay current on advances in ophthalmology and gene therapy to help guide program strategy
- Report to the Vice President of Clinical Development
- Provide strategic leadership on clinical development plans, study design, endpoint selection, regulatory strategy, and key program milestones
Requirements
What you’ll need- Advanced scientific or medical degree preferred (MD, PharmD, PhD, or equivalent experience)
- 5+ years of clinical development experience in biotech or pharma
- Ophthalmology experience required
- Gene therapy experience required
- Retina experience required
- Glaucoma experience preferred but optional
- Experience preparing and reviewing a broad range of clinical and regulatory documents
- Strong understanding of clinical trial design and GCP guidelines
- Excellent communication, leadership, and collaboration skills
- Proven experience leading delivery through collaboration with internal organization and external vendors
- Comfortable operating in a dynamic, hands-on biotech environment
- Strong written and spoken English skills
- Swiss working permit or EU citizenship eligible to work in Switzerland
Benefits
Comp & perks- Opportunity to help develop breakthrough therapies for patients with serious vision-threatening diseases
- Work alongside a passionate, highly experienced team at the forefront of ophthalmology innovation
- Meaningful impact in a growing biotech company
- Collaborative, entrepreneurial culture where science and innovation drive decision-making
