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Principal Pathologist

WuXi AppTec
Posted 18 days ago, valid for 12 days
Salary

Competitive

Contract type

Full Time

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Sonic Summary

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  • WuXi AppTec is seeking a Pathologist to contribute to Toxicology, Safety, and Biocompatibility activities, with responsibilities including study evaluation and pathology reporting.
  • The position can be either on-site at the Natick facility or remote, depending on the candidate's experience and level of independent diagnosis.
  • Candidates must hold a DVM or equivalent, be ACVP Board Certified, and have at least 10 years of toxicological pathology experience in the CRO or pharmaceutical industry.
  • The role offers the potential for hiring at either the Senior or Principal level based on qualifications.
  • Salary details are not specified, but the position requires significant expertise in pathology and compliance with GLPs.

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.




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