Associate Director, Clinical Pathologist

Regeneron

. Serve as a scientific leader supporting nonclinical drug development across multiple therapeutic areas .

Posted 9/30/2026full-timeRemote • United StatesSenior💰 $176,100 - $287,300 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in Clinical Pathology with a focus on nonclinical drug development, integrating clinical and anatomic pathology data to support therapeutic advancements. Proven ability to mentor junior pathologists and collaborate effectively within cross-functional teams.

Highest-signal resume keywords

DVM (Or Equivalent) With ACVP CertificationGLP And Non-GLP Clinical Pathology Data InterpretationExperience With Animal Models Of Human DiseasesMentoring Junior PathologistsCross-Functional Team Collaboration

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical PathologyPharmacologyToxicologyData InterpretationGLP Toxicology StudiesPK StudiesScientific Strategy DevelopmentProblem SolvingClinical Pathology Endpoints EvaluationAnatomic Pathology Integration

Soft Skills

Clear CommunicationConcise WritingTeam Contribution

Certifications & Qualifications

ACVP Certification In Clinical PathologyAdditional Certification In Anatomic Pathology

Industry Keywords

Nonclinical Drug DevelopmentPharma/BiotechCRO SettingTherapeutic AreasSafety Studies

About the role

Key responsibilities & impact

Serve as a scientific leader supporting nonclinical drug development across multiple therapeutic areas
Work independently and as part of integrated discovery and development teams
Interpret pharmacologic and toxicity-related findings to advance promising therapeutics through Regeneron’s pipeline
Determine and evaluate clinical pathology-related endpoints in pharmacology and toxicology studies
Guide decision-making based on clinical pathology findings
Collaborate with anatomic pathologists, toxicologists, and researchers within Regeneron
Partner with CROs to provide scientific peer review of nonclinical safety studies
Manage Clinical Pathology support for selected therapeutic focus areas
Mentor junior Pathologists
Support drug molecule efficacy and safety studies, including GLP toxicology and PK studies

Requirements

What you’ll need

DVM (or equivalent) with ACVP certification in Clinical Pathology required
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
Experience 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 broader understanding of pathology-related issues influencing drug development outcomes
Additional certification in Anatomic Pathology is nice to have
Background checks may be conducted, including verification of identity, right to work, and educational qualifications

Benefits

Comp & perks

Annual bonuses or other incentive plans
Equity awards
Pension or retirement benefits
401(k) company match
Health and wellness programs
Fitness centers
Medical, dental, vision, life and disability insurance benefits
Paid time off
Family support benefits
Reasonable accommodation during the recruitment process where required