Associate Director, Clinical Pathologist

About the role

Associate Director of Pathology has primary responsibility to support drug molecule efficacy and safety studies in a variety of therapeutic focus areas (TFAs). The successful candidate will also provide Clinical Pathology support for GLP toxicology and PK studies of Regeneron molecules. The Associate Director will be expected to manage Clinical Pathology support to selected TFAs, and mentor junior Pathologists.

Responsibilities

• Serve as a scientific leader supporting nonclinical drug development across multiple therapeutic areas.
• Work both independently and as a part of integrated discovery and development teams to interpret pharmacologic and toxicity related findings and help advance promising therapeutics through Regeneron's pipeline.
• Determine and evaluate clinical pathology-related endpoints in pharmacology and toxicology studies and guide decision making.
• Collaborate closely with anatomic pathologists, toxicologists, and researchers within Regeneron.
• Partner with CRO partners in providing scientific peer review of nonclinical safety studies.

Requirements

• DVM (or equivalent) with ACVP certification in Clinical Pathology required (strong preference for PhD in Pathology, Immunology, or related field).
• Minimum 3 years of industry experience interpreting GLP and non‑GLP clinical pathology data in nonclinical studies and supporting discovery research in a pharma/biotech or CRO setting.
• Additional certification in Anatomic Pathology is a nice‑to‑have.

Skills

• Experience with integrating clinical and anatomic pathology data.
• Experience with animal models of human diseases.
• Clear, concise oral and written communication skills.