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Pathologist

WuXi AppTec Group

Bristol

Remote

GBP 80,000 - 100,000

30+ days ago

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Job summary

An innovative firm is seeking a skilled pathologist to join their team, contributing to critical toxicology and biocompatibility studies. This role involves performing detailed examinations, writing comprehensive reports, and collaborating with sponsors to ensure the highest standards of safety and compliance in drug development. The ideal candidate will possess a Doctor of Veterinary Medicine degree and ACVP Board Certification, along with experience in the pharmaceutical industry. This position offers flexibility, with the potential for remote work, making it an exciting opportunity for professionals looking to make a significant impact in the field.

Qualifications

  • DVM or equivalent with ACVP Board Certification required.
  • 2+ years of experience in toxicological pathology in CRO or pharma.

Responsibilities

  • Conduct macroscopic and microscopic examination for preclinical studies.
  • Communicate with sponsors about pathology reports and results.
  • Ensure compliance with GLPs and conduct training for junior pathologists.

Skills

Oral Communication

Written Communication

Adaptability

Teamwork

Education

DVM (Doctor of Veterinary Medicine)

ACVP Board Certification

Tools

Microsoft Excel

Microsoft Word

Microsoft Outlook

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 position has the flexibility to be based in Plainsboro, NJ or Natick, Massachusetts. If hired at a senior or principal level, this job can be 100% remote/work from home.

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
  • Communicate with sponsors to answer questions and discuss results regarding the pathology report.
  • Provide consultation to Study Directors on studies.
  • 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
  • Ensure the compliance of various GLPs, comply protocol and SOPs during study activities
  • Conduct planned, long-term education and training for junior pathologists
  • 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.
  • 2+ years of toxicological pathology experiences in the CRO or pharmaceutical industry

Knowledge / Skills / Abilities:

  • Proficient in Oral & Written communication skills.
  • Proficient in Microsoft (Excel, Word, Outlook).
  • Need to be able to read, write and understand English.
  • Adaptability, flexibility and ability to manage changing priorities.
  • Self-responsibility and independence, while at the same time being a team player.
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