WuXi AppTec
Principal Pathologist
WuXi AppTec, Phila, Pennsylvania, United States, 19117
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 fornonclinical studies spanning all phases of drug developmentfor pharmaceutical industries.
Responsibilities
Essential Job Functions:
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 Principle 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 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.
10+ years of toxicological pathology experiences 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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Job Locations US
Job ID 2024-13327
WuXi AppTec Pathologists contribute to a wide range of critical activities within Toxicology, Safety, and Biocompatibility. Testing including but not limited to study evaluation fornonclinical studies spanning all phases of drug developmentfor pharmaceutical industries.
Responsibilities
Essential Job Functions:
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 Principle 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 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.
10+ years of toxicological pathology experiences 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.
Need help finding the right job?
We can recommend jobs specifically for you!
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Job Locations US
Job ID 2024-13327