Director, Clinical Scientist

Role: Senior Clinical Scientist overseeing ophthalmology product development, focusing on clinical trial design, data analysis, and regulatory documentation. Responsibilities include preparing clinical protocols, reports, and submissions, managing trial data review, ensuring compliance with GCP and regulatory standards, and supporting site initiation and recruitment strategies. Collaborates across clinical development teams and CROs, preparing materials for regulatory agencies and scientific publications. Requirements: PhD or PharmD in life sciences; 10+ years in clinical research, especially in ophthalmology and drug/device combination products; expertise in all clinical development phases, regulatory submissions, and GCP principles. Preferred: experience in ophthalmic therapeutics, strong scientific literature interpretation, and cross-functional teamwork skills. HighValue: ophthalmology, drug/device combination, clinical trial phases (all), regulatory submissions, GCP compliance, global trial management. WorkSetup: remote; no travel specified.