Principal Pathologist

WuXi AppTec Group; Natick (MA); On-site; USD 180,000 - 250,000; Full time

Job summary

WuXi AppTec Group is seeking a senior/pathologist to join our Natick, MA team. The role can be on-site at the Natick facility or remote depending on experience and qualifications.

The ideal candidate will hold a DVM and ACVP Board Certification, with 10+ years in toxicological pathology within CRO or pharmaceutical settings. Responsibilities include pathology evaluation, reports, peer review, mentorship, and sponsor communication.

Qualifications

• DVM (Doctor of Veterinary Medicine) or equivalent.
• ACVP Board Certification is required.
• 10+ years of toxicological pathology experience in the CRO or pharmaceutical industry.

Responsibilities

• Attend key activities of preclinical studies regarding pathology, perform macroscopic and microscopic examination, evaluate data and write pathology reports.
• Participate in pathology peer review as SOP and protocol requires.
• Act as Principal Investigator for pathology-related activities.
• Conduct long-term education and training for junior pathologists.
• Communicate with sponsors to discuss results and answer questions on pathology reports.
• Provide consultation to Study Directors on studies.
• Ensure GLP compliance and adherence to protocols during study activities.
• Conduct toxicology and medical device studies in compliance with GLP/CNAS.

Education

DVM (Doctor of Veterinary Medicine)

ACVP Board Certification

Job description

Overview

WuXi AppTec Pathologists contribute to a wide range of critical activities within Toxicology, Safety, and Biocompatibility. Testing including but not limited to study evaluation for nonclinical studies spanning all phases of drug development for pharmaceutical industries.

This role is either on-site at our Natick facility or remote (this determination will depend on experience and a candidate’s level of independent diagnosis). Also, we can hire at the Senior or Principal level depending on a candidate's experience and qualifications.

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

Qualifications

Experience / Education:

• DVM (Doctor of Veterinary Medicine) or equivalent
• ACVP Board Certification is required
• 10+ years of toxicological pathology experience in the CRO or pharmaceutical industry

This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. Employees holding this position will be required to perform any other job‑related duties as requested by Management.

An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.