Associate Director Pathology

Associate Director of Pathology

The Associate Director of Pathology has primary responsibility to support drug molecule efficacy and safety studies in a variety of therapeutic focus areas. 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.

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.

This job might be for you if you have:

• 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
• Ability to contribute to scientific strategy, problem solving, and the broader understanding of pathology-related issues that influence drug development outcomes.

In order to be considered for this role, you must have:

• DVM (or equivalent) with ACVP certification in Clinical Pathology (strong preference for PhD)
• Minimum 3 years of experience interpreting GLP and non GLP clinical pathology data in nonclinical studies and supporting discovery research in a pharma/biotech or CRO setting.
• Preferred qualifications: PhD in a scientific field and/or Certification in Anatomic Pathology