Associate Director Pathology

Regeneron Pharmaceuticals • Tarrytown, GA

8d • $176,100 - $287,300 • Onsite

About The Position

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 histopathology evaluation support and immunopathology oversight for GLP toxicology and PK studies of Regeneron molecules. The Associate Director will be expected to manage Pathology support to selected TFAs, act as lead Pathologist on project teams and mentor junior Pathologists. A Typical day in this role may look like: 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. Determining and evaluating clinical pathology related endpoints in pharmacology and toxicology studies and guiding decision making. Collaborate closely with anatomic pathologists, toxicologists, and researchers within Regeneron. Partner with our CRO partners in providing scientific peer review of nonclinical safety studies.

Requirements

• DVM (or equivalent) with ACVP certification in Clinical Pathology or PhD in a scientific field
• Minimum 3 years of experience interpreting GLP and non GLP clinical pathology data in nonclinical studies and supporting discovery research in pharma/ biotech or CRO.
• Certification in Anatomic Pathology
• Experience with integrating clinical and anatomic pathology data
• Experience with animal models of human diseases
• Clear, concise oral and written communication skills
• Demonstrated ability to contribute to cross functional teams contributing to scientific strategy, problem solving, and the broader understanding of pathology-related issues that influence drug development outcomes.

Responsibilities

• Support drug molecule efficacy and safety studies in a variety of therapeutic focus areas (TFAs).
• Provide histopathology evaluation support and immunopathology oversight for GLP toxicology and PK studies of Regeneron molecules.
• Manage Pathology support to selected TFAs.
• Act as lead Pathologist on project teams.
• Mentor junior Pathologists.
• 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.

Benefits

• health and wellness programs (including medical, dental, vision, life, and disability insurance)
• fitness centers
• 401(k) company match
• family support benefits
• equity awards
• annual bonuses
• paid time off
• paid leaves (e.g., military and parental leave)

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Education Level: Ph.D. or professional degree