Job Overview

As a Research Scientist for our Discovery team at the Senneville location, you will serve as a Study Scientist or Principal Investigator responsible for the design, conduct and reporting of Laboratory Sciences studies efficiently, profitably and with the maximum scientific quality.

In this role, primary responsibilities include:

• Design, write, review, and edit study plans, amendments and study schedules that define and schedule all study activities;
• Oversee and coordinate all aspects of study related Laboratory Sciences procedures, whether performed within the department or by service departments;
• Analyze scientific problems, troubleshoot analytical methods and technical issues;
• Write scientific documents, review and interpret the raw data;
• Write, review, and edit stand-alone contributing Scientist draft and/or final reports that document all study related procedures and results;
• Prompt verbal or written communications with Study Directors and/or Sponsor on study related business in a timely manner;
• Ensure the accuracy and completeness of project cost estimates;
• Notify the Principal Scientist and/or the Scientific Director of scientist or technical problems as soon as they become apparent.

Key Elements

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

• Holder of a Master in Immunology or any other related discipline with a minimum of 3 to 5 years' experience working in a Scientific position;
• PhD in Immunology or any biological related discipline;
• Experience in the development, optimization and use of multi-parameter flow cytometry;
• Experience with the Cytek Spectral flow cytometer platform is an asset;
• Experience with microscopy and live cell imaging is an asset;
• Experience with immunoassay techniques (ELISAs, ECLs, Luminex) and in-vitro cell-based assays (ELISpot, primary culture, co-culture, scaffold-based culture, spheroid, organoid and organ-on-chip) is an asset;
• Outstanding organizational skills;
• Good interpersonal and communication skills;
• Strong problem-solving skills;
• Work with precision, pay attention to detail and strive for quality work.

Role Specific Information:

• Location: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
• Transportation: We offer a free shuttle service from the Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site. Free parking. Electric vehicle charging station;
• Annual bonus based on performance;
• Schedule: Monday to Friday, 9am to 5:15pm;
• 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 development training;
• 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.