Regeneron
AssociateDirectorPathology
Neural analysis suggests this role is
optimal for Director candidates.
“Associate Director Pathology at Regeneron. Skills: Clinical Pathology, Drug development, Toxicology studies. Support drug molecule efficacy studies. Support drug molecule safety studies”
Industry & Context.
Problem solving
What They're Looking For.
Must Have
DVM or equivalent, ACVP certification in Clinical Pathology, 3 years interpreting GLP/non-GLP clinical pathology data, 3 years supporting discovery research, Experience in pharma/biotech or CRO setting
Nice to Have
PhD in a scientific field, Certification in Anatomic Pathology
What You'll Do.
Support drug molecule efficacy studies
Support drug molecule safety studies
Provide Clinical Pathology support
Manage Clinical Pathology support
Serve as scientific leader
Support nonclinical drug development
Interpret pharmacologic findings
Interpret toxicity findings
Advance therapeutics through pipeline
Determine clinical pathology endpoints
Evaluate clinical pathology endpoints
Guide decision making
Partner with CRO partners
Provide scientific peer review
How You'll Work.
Team & Collaboration
Integrated discovery teams; Development teams; Anatomic pathologists; Toxicologists; Researchers; CRO partners
Communication Scope
Clear oral communication; Concise written communication
Full Job Description
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. **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 Does this sou
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