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Altasciences

Integrated CRO for early-phase drug development

Toxicologic Pathologist

Biology & BiotechConfirmed live in the last 24 hours
Full-timeColumbia, MO, USA$170k - $210kRemote

About the Job

Requirements

  • A D.V.M. or equivalent as listed by AVMA ECFVG is required.
  • At least five years of toxicologic pathology experience in a Good Laboratory Practice (GLP) environment is required.
  • Diplomate status with A.C.V.P., J.C.V.P., E.C.V.P., or R.C.P. is required.
  • Proficiency with Microsoft Word, Excel, Outlook, and PowerPoint is required.
  • Ability to read and interpret technical documents and industry-specific manuals is required.
  • Ability to write advanced reports and correspondence is required.
  • Excellent verbal and written communication skills are required.
  • Well-developed interpersonal skills are required.
  • Personal and professional integrity and discretion in handling confidential information are required.
  • Ability to develop trusting relationships to gain support and achieve results is required.
  • Ability to manage multiple conflicting priorities is required.
  • Ability to work independently, stay motivated, take initiative to identify and anticipate client needs, and make implementation recommendations is required.

Responsibilities

  • Perform duties as a study pathologist or peer reviewer on preclinical toxicology studies.
  • Diagnose the presence and stage of disease or toxicity using laboratory techniques and patient specimens, and study its nature, cause, and development.
  • Perform macroscopic and microscopic tissue evaluations and interpret assigned studies.
  • Assist with necropsy supervision and gross pathology interpretation.
  • Guide laboratory staff in sample collection and technical development.
  • Write comprehensive report narratives detailing all test article effects.
  • Enter pathology findings into the data-capturing system.
  • Work with study directors as needed to ensure data is accurately integrated into study reports.
  • Provide training, technical guidance, and leadership to laboratory staff, pathology trainees, and less experienced pathologists.
  • Maintain up-to-date knowledge of toxicologic pathology.
  • As needed, serve as principal investigator for contract pathology work, participate as an observer in pathology working groups, and consult on pathology-related issues.
  • Provide scientific expertise for experimental design and other aspects of research studies as needed.
  • Act as the pathology representative for sponsors.
  • Provide mentorship through scientific reviews of assigned studies for less experienced pathologists.
  • Support the establishment or refinement of significant operational or scientific improvements within pathology.

Desired Qualifications

  • Relevant industry experience is a plus.

About the Company

Altasciences

Integrated CRO for early-phase drug development

Altasciences provides integrated early-stage drug development services, covering preclinical testing, early clinical trials, and contract manufacturing. It functions as a single, in-house CRO that coordinates discovery support, safety testing, clinical research, and manufacturing to streamline a program from start to early proof of concept. The company differentiates itself by offering an end-to-end, one-stop path rather than requiring clients to contract multiple vendors. Its goal is to help innovator programs move quickly and efficiently through early development to speed up decision making and progression to later-stage trials.

Company size
1,001-5,000
Company stage
Early VC
Total funding
$6.7M
Headquarters
Laval, Canada
Founded
1976

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