Responsibilities
- As a study pathologist, attend all key activities of preclinical studies regarding pathology, perform macroscopic and microscopic examination, evaluate pathological data and write comprehensive pathology report
- Function as a Peer review pathologist, take part in pathology peer review as SOP and protocol required
- Function as a Principal Investigator, responsible for pathology-related activities
- Conduct planned, long-term education and training for junior pathologists
- Communicate with sponsors to answer questions and discuss results regarding the pathology report
- Provide consultation to Study Directors on studies
- Ensure the compliance of various GLPs, comply with protocol and SOPs during study activities
- Responsible for conducting toxicology and medical device studies in compliance with GLP/CNAS
- Perform other duties as assigned
Requirements
- DVM (Doctor of Veterinary Medicine) or equivalent
- ACVP Board Certification is required
- 10+ years of toxicological pathology experience in the CRO or pharmaceutical industry
Work Arrangement
On-site — Natick