Research Fellow, Pharma Toxicology

Role: Lead pharmacotoxicology expert supporting pharmaceutical development and lifecycle management for eye health products, with a focus on nonclinical safety assessments. Responsibilities: develop and oversee nonclinical safety strategies for pharmaceuticals, OTC, and consumer products; ensure alignment of development plans with regulatory and product objectives; interpret and communicate toxicology data for regulatory submissions and product launches; mentor junior staff and manage toxicology team; stay current with industry standards and update practices accordingly; author and review scientific documents; collaborate cross-functionally with R&D, Regulatory, Quality, and global sites; improve departmental procedures. Requirements: Ph.D. in Toxicology or related field; 12+ years in pharma industry; experience with ophthalmology drug development preferred; DABT certification desirable. HighValue: ophthalmology, pharmaceutical development, nonclinical safety, regulatory compliance, cross-functional leadership. WorkSetup: remote US location.