Senior Veterinary Clinical Pathologist, Preclinical Safety

BioSpace; North Chicago (IL); On-site; USD 180,000 - 240,000; Full time

Benefits offered by this job

Comprehensive benefits

Long-term incentive programs

401(k) plan

Job summary

AbbVie seeks an on-site Board-Certified Veterinary Clinical Pathologist for the Department of Pathology in Preclinical Safety (PCS). The role focuses on evaluating clinical pathology data, preparing interpretive text for regulatory toxicity studies, and collaborating with cross-functional teams to support new therapeutics.

The candidate will review partner reports, communicate findings clearly to diverse scientific groups, and contribute to regulatory documents while working with a multi-site

Qualifications

• DVM or equivalent degree required.
• ACVP (Clinical Pathology) board certification required.
• PhD in pathology is desirable.
• Experience in pharmaceutical industry or CRO is a plus.

Responsibilities

• Evaluate clinical pathology data and integrate findings into descriptive text for regulatory toxicity study reports.
• Review clinical pathology reports from partner organizations.
• Clearly communicate key pathology findings to diverse scientific teams.
• Serve as SME to inform/optimize pathology support for preclinical programs.
• Coordinate with biomarker scientists, pathologists, toxicologists and other scientists across sites.
• Contribute to regulatory submissions and related documentation.
• Collaborate with on-site and remote teams to optimize laboratory capabilities.

Skills

Critical thinking

Communication skills

Strategic planning

Cross-functional collaboration

Team leadership

Education

DVM or equivalent

ACVP Certification

PhD in pathology

Job description

AbbVie seeks an on-site Board-Certified Veterinary Clinical Pathologist for the Department of Pathology in Preclinical Safety (PCS). The role focuses on evaluating clinical pathology data, preparing interpretive text for regulatory toxicity studies, and collaborating with cross-functional teams to support new therapeutics.

The candidate will review partner reports, communicate findings clearly to diverse scientific groups, and contribute to regulatory documents while working with a multi-site