Senior Veterinary Pathologist

Charles River

$110K — $130K *
Healthcare
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Doctorate degree (D.V.M/V.M.D.) from an accredited veterinary school or equivalent.
  • 6+ years of post-D.V.M pathology experience.
  • Board certification with A.C.V.P or E.C.V.P required.
  • Working knowledge of clinical pathology preferred.
  • Demonstrated success in technical proficiency and scientific creativity.
  • Ability to analyze diverse data and exercise sound judgement.
  • Proficiency in related computer applications.

Responsibilities

  • Perform macroscopic and microscopic tissue evaluations.
  • Enter pathology findings into data systems.
  • Write comprehensive reports on test article effects.
  • Train and guide laboratory staff and less experienced pathologists.
  • Stay updated on toxicologic pathology developments.
  • Market services to customers and ensure their satisfaction.
  • Act as core pathologist for important sponsors.

Benefits

  • Competitive benefits from day one.
  • Paid yearly ACVP / ECVP license.
  • On-site gym access.
  • Employee and family assistance program.
  • Four weeks of vacation and ten personal days.
  • Annual performance-based bonus.
  • Free parking and electric vehicle charging station.
Full Job Description
Job Overview

As a Senior Veterinary Pathologist for our team at the Senneville location, you will be responsible for applying advanced scientific knowledge to perform microscopic evaluation of tissues, and for recording results, preparing complex reports delineating pathological findings, and assisting with necropsy supervision.

In this role, primary responsibilities include:

  • Perform macroscopic and microscopic tissue evaluation and interpretation of assigned studies;
  • Enter pathology findings in data capturing systems;
  • Write comprehensive report narratives detailing all test article effects. As needed, work with study directors to ensure data is accurately integrated into study reports;
  • Provide training, technical guidance and leadership to laboratory staff and may provide training, guidance, and leadership to less experienced pathologists;
  • Maintain an up-to-date knowledge in toxicologic pathology;
  • Work directly with customers as needed to market company services and to assure customer satisfaction Participate to global CRL committees/projects as needed;
  • Act as "core pathologist" for important sponsors;
  • Serve as a consultant in pathology-related issues;
  • Provide advanced scientific expertise for experimental design and other aspects of research studies as needed.
  • May serve as principal investigator for contract pathology work;
  • May function as a peer review pathologist or may participate in a pathology working group (PWG) as a pathologist;
  • May perform scientific review of reports;
  • May assist with necropsy supervision.


Key Elements

We are looking for the following minimum qualifications for this role:

  • Doctorate degree (D.V.M/V.M.D.) from an accredited veterinary school, or acceptable international equivalent in veterinary medicine;
  • 6 or more years of pathology experience post-D.V.M;
  • Working knowledge of clinical pathology preferred;
  • Board certification with the American College of Veterinary Pathologists (A.C.V.P.) or European College of Veterinary Pathologists (E.C.V.P) required to enter the level grade;
  • Demonstrated success in technical proficiency, scientific creativity, collaboration with others and independent thought;
  • Ability to work on problems of diverse scope in which analysis of data requires evaluation of multiple factors;
  • Ability to exercise judgement within generally defined practices and policies in selecting methods or techniques for obtaining solutions;
  • Working knowledge of related computer applications.

Please note that upon being hired, you will have to undergo an annual tuberculosis test covered by the company.

Role Specific Information:

  • Location: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
  • Transportation: We offer a shuttle service from Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site. In addition, the site is accessible from the Anse-à-l'Orme REM station via STM bus services.
  • Free parking. Electric vehicle charging station;
  • Annual bonus based on performance;
  • Schedule: Monday to Friday, daytime;
  • Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

  • We offer competitive benefits and advantages from day one to support your well-being;
  • Paid ACVP / ECVP yearly license;
  • Free gym on site;
  • Employee and family assistance program;
  • Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
  • Access to a doctor and various health professionals (telemedicine);
  • 4 weeks' Vacation & 10 Personal day policy;
  • Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.

About Charles River
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.

With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.

At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

We're committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.

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