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Clinical Project Director Jobs in Quebec (NOW HIRING)

As needed, work with study directors to ensure data is accurately integrated into study reports ... Participate to global CRL committees/projects as needed; * May serve as principal investigator for ...

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Reporting to the Associate Director, you will cultivate a strong team identity with personalized ... Product and Project Ownership * Define, prioritize, and execute the team's roadmap in collaboration ...

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Clinical Project Director information

What is the difference between Clinical Project Director vs Clinical Project Manager?

AspectClinical Project DirectorClinical Project Manager
ResponsibilitiesOversees multiple projects, strategic planning, high-level decision makingManages individual projects, coordinates teams, ensures project milestones
Required CredentialsTypically requires a clinical research degree, extensive experience, and certifications like PMPRequires a relevant degree, experience in clinical trials, and often PMP or similar certifications
Work EnvironmentSenior leadership in pharmaceutical or biotech companies, CROsProject teams within clinical research organizations or pharmaceutical companies

The Clinical Project Director focuses on strategic oversight and managing multiple projects at a higher level, while the Clinical Project Manager handles day-to-day project execution and team coordination. Both roles require relevant clinical research experience and certifications, but the Director role involves broader responsibilities and strategic planning.

What are the most commonly searched types of Clinical Project jobs in Quebec?

The most popular types of Clinical Project jobs in Quebec are:

What job categories do people searching Clinical Project Director jobs in Quebec look for?

The top searched job categories for Clinical Project Director jobs in Quebec are:

Infographic showing various Clinical Project Director job openings in Quebec as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.

Veterinary Pathologist II

Charles River Laboratories, Inc.

Senneville, QC • On-site

Full-time

Medical, Retirement, PTO

Posted 3 days ago

New


Charles River Laboratories rating

8.4

Company rating: 8.4 out of 10

Based on 94 frontline employees who took The Breakroom Quiz

22nd of 86 rated pharmaceutical


Job description

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we'll help you build a career that you can feel passionate about.

Job Overview

As a Veterinary Pathologist II for our team at the Senneville location, you will be responsible for independently performing microscopic evaluation of tissues, recording results, preparing 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;
  • Assist with necropsy supervision;
  • 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 with customers as needed to market company services and to assure customer satisfaction;
  • Participate to global CRL committees/projects as needed;
  • May serve as principal investigator for contract pathology work;
  • May participate in pathology working group (PWG) as an observer;
  • May serve as a consultant in pathology-related issues;
  • May provide scientific expertise for experimental design and other aspects of research studies as needed.
Job Description

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;
  • 3 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-a-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.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

For more information, please visit www.criver.com.


What Charles River Laboratories employees say

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About Charles River

Sourced by ZipRecruiter

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 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 supported the development of 86% of the drugs approved by the FDA in 2021.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

Wilmington, MA, US

Year founded

1947