Latigo Creative

Director

• Serve as the nonclinical safety/toxicology subject matter expert on multidisciplinary project teams
• Provide integrated assessments of nonclinical data and evaluate overall risk/benefit profiles
• Contribute to development candidate selection and overall program strategy
• Design, oversee, and monitor nonclinical safety studies
• Analyze and interpret nonclinical study data to support program decisions
• Author and review nonclinical sections of regulatory documents
• Collaborate closely with Discovery, DMPK, Clinical Pharmacology, Clinical Development, and Regulatory teams

Associate Director, Toxicology