Responsibilities:
- Clinical pathology assessment of preclinical results for platform and program support
- Review non-GLP and GLP study clinical pathology data
- Interpret and report findings and their significance to program teams and broader audiences via descriptions, data tables, and scientific presentations
- Contribute clinical pathology reports and/or reviews for regulatory filings
- Consult with internal and external stakeholders on preclinical study design and interpretation
- Participate in program and platform meetings
- Mentor the clinical pathology scientist; collaborate with pathology team members to support nonclinical data generation and analysis
- Share biomarker and translational expertise across Research and Early Development
- Participate in group, department, and company meetings and activities
Qualifications:
- 15+ years of experience as a pathologist in biotech, pharma, or at a CRO
- Veterinary degree and ACVP/ECVP board certification in clinical pathology; PhD preferred but not required with relevant pathology experience
- Demonstrated scientific curiosity via publication and/or presentation record
- Strong interest in areas of Alnylam research emphasis (demonstrated experience preferred)
- Strong communication skills
- Ability/interest to travel for essential company activities
- Onsite/hybrid role in Cambridge, MA