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
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.
Skills Required
- Doctor of Veterinary Medicine degree or equivalent
- ACVP Board Certification
- 10 or more years of toxicological pathology experience in a CRO or pharmaceutical industry
What We Do
WuXi Chemistry, a business division of WuXi AppTec, provides contract services for new drug development from discovery to commercial. Our unique CRDMO model offers an integrated solution combining traditional CRO (contract research organization), CDMO (contract development and manufacturing organization) and CMO (contract manufacturing organization) services under one roof. As a world leading chemistry service organization, WuXi Chemistry have over 24,000+ employees from our 16 research, development or manufacturing sites worldwide, serving over 2,000+ clients from top pharma to virtual biotech companies. Our services cover all categories for all synthetic molecular modalities, meeting any material requirement at any scale. Visit STA, CRDMO for small molecule drugs: https://stapharma.com Visit WuXi TIDES, CRDMO for oligonucleotide, peptide, and conjugates: https://tides.wuxiapptec.com/
