Director, Translational Pathology & Safety

askbio; Durham (NC); On-site; USD 180,000 - 250,000; Full time

Job summary

AskBio Inc. seeks a Director of Pathology to lead Translational Medicine Safety (anatomic and clinical pathology & toxicology) across multiple drug candidates.

You will act as PI for non‑GLP and GLP studies, ensuring high‑quality pathology assessments to support regulatory submissions (IND/CTA/NDA) and cross‑functional dissemination of findings. The role requires deep expertise in nonclinical safety, histopathology, and regulatory biology, with leadership across Discovery, Product Development,

Qualifications

• DVM with 6+ years of post‑graduate experience in pharma/biotech/academia.
• Board certification in Veterinary Pathology (DACVP or ECVP) required or equivalent.
• Experience integrating pathology data into clinical development decisions.
• Familiarity with regulatory submissions (IND/CTA/NDA) and tox/pathology reporting.
• Strong leadership and cross‑functional collaboration skills.

Responsibilities

• Lead Translational Medicine Safety (pathology & toxicology) strategy for nonclinical programs.
• Provide pathology support including histopathology reviews and data interpretation.
• Serve as Principal Investigator for non-GLP and GLP studies and coordinate CROs.
• Guide study design, execution, and reporting for regulatory submissions.
• Mentor and manage histopathology staff and collaborators; drive SOPs and quality.
• Communicate regulatory findings clearly to internal teams and Health Authorities.

Skills

Project management

Regulatory knowledge

Nonclinical safety assessment

Leadership

Written communication

Education

DVM

Board Certification in Veterinary Pathology (DACVP/ECVP)

Master’s or PhD in a scientific discipline

Tools

LIMS

Digital/pathology imaging (H&E/IHC)

Job description

AskBio Inc. seeks a Director of Pathology to lead Translational Medicine Safety (anatomic and clinical pathology & toxicology) across multiple drug candidates.

You will act as PI for non‑GLP and GLP studies, ensuring high‑quality pathology assessments to support regulatory submissions (IND/CTA/NDA) and cross‑functional dissemination of findings. The role requires deep expertise in nonclinical safety, histopathology, and regulatory biology, with leadership across Discovery, Product Development,