Principal Pathologist (Toxicology)

TL;DR

Principal Pathologist (Toxicology): Conducting comprehensive nonclinical study evaluations and pathology assessments for pharmaceutical drug development with an accent on GLP compliance and peer review. Focus on performing macroscopic and microscopic examinations, providing expert consultation to Study Directors, and mentoring junior pathology staff.

Location: Must be based in the United States (On-site at Natick facility or remote depending on experience).

Company

A global provider of R&D and manufacturing services for the pharmaceutical, biotech, and medical device industries.

What you will do

• Perform macroscopic and microscopic examinations for preclinical studies.
• Evaluate pathological data and author comprehensive pathology reports.
• Serve as a Peer Review Pathologist and Principal Investigator for pathology-related activities.
• Provide expert consultation to Study Directors regarding study outcomes.
• Communicate directly with sponsors to discuss findings and address inquiries.
• Lead education and training initiatives for junior pathologists.

Requirements

• DVM (Doctor of Veterinary Medicine) or equivalent degree required.
• ACVP Board Certification is required.
• 10+ years of toxicological pathology experience in CRO or pharmaceutical industry.
• Strong knowledge of GLP/CNAS compliance standards.
• Ability to work independently and manage complex pathology workflows.

Culture & Benefits

• Opportunity to work on critical drug development and safety studies.
• Professional development through peer review and leadership responsibilities.
• Equal Opportunity Employer committed to a diverse and inclusive workplace.