Generate, evaluate, and interpret GLP and non-GLP pathology data for assigned studies, including determination of adversity where appropriate.
Conduct and/or support postmortem phases of toxicology studies, including pathology peer and scientific review.
Contribute to integrated nonclinical data analyses, interpretation, human risk assessment, and high-quality reporting.
Support regulatory submissions through preparation and review of pathology related documentation.
Serve as a pathology contributor or early project team representative for preclinical safety.
Participate in nonclinical study design, protocol writing, and review.
Monitor and review pathology procedures and data generated by CROs and external partners.
Provide scientific and technical interpretation using expertise in clinical pathology, histopathology, histochemistry, morphology, image analysis, transcriptomics, electron microscopy, and related techniques.
Identify and contribute to novel projects or emerging scientific/technical areas aligned with departmental strategy.
Maintain current knowledge of scientific advances, technologies, and methodologies.
Collaborate across therapeutic areas and modalities; identify key connection points to enable project progression.
Essential Requirements:
Education: DVM (or equivalent, e.g., BVSc)
Graduate training in pathology
Preferred candidate will also have a PhD in a relevant biological or toxicologic field and 2 plus years of experience in toxicologic pathology; 5 plus years to be considered at the Associate Director level
To be considered at the Associate Director level you will also have:
Demonstrated team leadership
Ability to supervise direct and develop others
Experience leading programs, platforms, or initiatives
This is a dual posting. The final level & title of the offer role would be determined by the hiring team based on the skills, experience & capabilities required to perform the role at the level the role has been offered.
The salary for this position is expected to range between:
Senior Principal Scientist I: $176,400 and $327,600 per year.
Associate Director: $185,500 and $344,500 per year.
EEO Statement:
Accessibility and reasonable accommodations
Salary Range
$176,400.00 - $327,600.00
Skills Desired
Analytical Thinking, Bioinformatics, Clinical Data Management, Colla
Benefits
Health insurance401(k)Paid time offEquity / stock options
Additional Information
Job Description Summary
#LI-Hybrid
Location: Cambridge, MA USA
Internal Title: Senior Principal Scientist or Associate Director
In this key role you will provide pathology subject matter expertise across drug discovery and development programs throughout the nonclinical and clinical development lifecycle, and/or contributes to department aligned technology development. You will also apply deep scientific judgment to assess the impact, limitations, and value of pathology data to advance projects, inform human risk assessment, and support Novartis portfolio strategy. You will have the opportunity to collaborate broadly across project teams, therapeutic areas, modalities, and external partners while maintaining compliance with Novartis policies, SOPs, GxP, One Quality, and health and safety requirements.
Job Description
Novartis · Cambridge (usa)