Provide scientific leadership across assigned ophthalmology clinical programs.
Translate scientific objectives into high-quality clinical development plans and trial designs.
Key Responsibilities:
Lead protocol development, study materials, and site feasibility assessments.
Oversee study conduct, data review, and interpretation of clinical efficacy and safety data.
Support regulatory interactions, submissions, and scientific communications.
Requirements:
Advanced degree (PharmD, PhD, OD, MS, MPH) with 7+ years of clinical research experience.
Experience in late-stage Phase 2/3 programs and ophthalmology preferred.
Strong knowledge of ICH-GCP and clinical trial processes.
Fully remote role in eligible US states with travel up to 15%.
Competitive compensation, health coverage, 401(k) matching, and generous PTO.
Not Specified The company is a clinical-stage organization advancing innovative regenerative therapies for significant unmet needs in ophthalmology. It fosters a collaborative, high-performance culture with mentorship and professional growth opportunities.
