Director

• Serves as the Non-Clinical Safety Assessment (toxicology) representative on interdisciplinary asset development teams (ADTs)
• Plans and executes non-clinical safety studies and assessments at appropriate stages to support asset progression through development and to meet project timelines
• Serving as the subject matter expert in the non-clinical field in meetings with internal/external stakeholders
• Author and review of non-clinical CTD modules for regulatory submission (e.g., IND, NDA)
• Provide scientific and strategic non-clinical safety (toxicological) input into Organon’s pipeline programs, business development activities, and existing product portfolio as an ADT representative
• Serve as a subject matter expert and/or provide technical area expertise for non-clinical development issues
• In conjunction with Non-Clinical Operations, coordinate non-clinical pharmacology and toxicology studies at Contract Research Organizations (CROs)

Associate Director, Non-Clinical Safety Assessment

Associate Director, Outcomes Research

Associate Director, Outcomes Research

Associate Director, Biopharmaceutics

Director, Clinical Pharmacology