Portfolio Pathologist (Anatomic)
$176,400–$327,600 year
On-site · Cambridge, Massachusetts, United States
Job Summary
Provide pathology subject matter expertise across drug discovery and development, spanning nonclinical and clinical development lifecycles, and contribute to department-wide technology development. Generate, evaluate, and interpret GLP and non-GLP pathology data, support postmortem toxicology phases, contribute to integrated nonclinical analyses and human risk assessment, and assist regulatory submissions. Serve as a pathology contributor or early project team representative for preclinical safety; participate in study design, protocol writing, and CRO data monitoring. Apply deep expertise in clinical pathology, histopathology, histochemistry, morphology, image analysis, transcriptomics, electron microscopy, and related techniques; identify novel projects aligned with departmental strategy; maintain knowledge of scientific advances; collaborate across therapeutic areas and modalities to enable project progression.
Required Qualifications
- Education: DVM (or equivalent, e.g., BVSc); graduate training in pathology.
- Pathology board certification (e.g., DACVP, ECVP, FRCPath).
- Preferred: PhD in relevant biological or toxicologic field.
- 5+ years experience in toxicologic pathology; 2+ years leadership/indirect supervision for Associate Director level consideration.
- Ability to supervise and develop others; experience leading programs/platforms/initiatives.
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