Research Fellow, Pharma Toxicology

Job Description

• Lead nonclinical safety assessment strategies for pharmaceuticals, over-the-counter products, and consumer goods in support of preclinical and lifecycle development.
• Oversee nonclinical data generation, interpretation, and communication for clinical development, regulatory submissions/registrations, product launch, market support, and compliance.
• Manage toxicology staff and mentor junior team members while leading departmental processes, standards, and best practices.
• Collaborate with Product Development, Clinical Development, Analytical Chemistry, Regulatory Affairs, Quality, Compliance, and international sites.
• Requires a Ph.D. in Toxicology or a related discipline, 12+ years of relevant pharmaceutical industry experience, U.S. work authorization without visa sponsorship, and preferably DABT certification and ophthalmology drug-development experience; US-Remote, $150,000–$200,000 starting pay.