Sr. Scientific Director, Toxicologic Pathology

We are seeking a Sr. Scientific Director, Toxicologic Pathology to lead nonclinical safety assessments for our pipeline. The ideal candidate will have a strong background in toxicologic pathology and experience in designing, overseeing, and interpreting GLP and non-GLP toxicology studies. This role requires excellent communication and leadership skills, with the ability to translate complex scientific findings into actionable insights for cross-functional teams.

Requirements

• DVM or PhD and 10+ years of industry experience in toxicologic pathology within biotech or pharmaceutical settings
• Board Certification by the American College of Veterinary Pathologists (ACVP) is required
• Expert knowledge in nonclinical safety assessment in drug development of small molecules, biologics, and peptides. Knowledge in gene therapy is plus
• Strong experience of designing, overseeing, and interpreting GLP and non-GLP toxicology studies
• Demonstrate ability to lead and manage internal team members, consultants, and CRO partnerships
• Deep understanding of regulatory requirements for nonclinical safety assessments, including experience with FDA, EMA, and other global health authorities
• Experience in responding to regulatory questions including discussion documents for various Health Authorities in support of discovery and development programs
• Expertise with the design and management of safety pharmacology and toxicology studies (GLP and non-GLP) supporting nonclinical and clinical development programs
• Excellent communication and leadership skills, with the ability to translate complex scientific findings into actionable insights for cross-functional teams
• Proven ability to thrive in a fast-paced, biotech environment

Benefits

• Retirement savings plan (with company match)
• Paid vacation
• Holiday and personal days
• Paid caregiver/parental and medical leave
• Health benefits to include medical, prescription drug, dental and vision coverage