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Research Assistant Lab Manager Jobs in Quebec (NOW HIRING)

... Clinical Research Unit (CRU). The role assists in preparing documents, tracking study progress ... Management System (CTMS). Primary Responsibilities: Administrative and Budget Support * Assist in ...

... Clinical Research Unit (CRU). The role assists in preparing documents, tracking study progress ... Management System (CTMS). Primary Responsibilities: Administrative and Budget Support * Assist in ...

The jobholder will be responsible for the following tasks: * Assist the City Manager's Office, in ... Conduct research, gather and collate information, data and various documents, from sources internal ...

Conduct applied research in the field of expertise that contributes to the programs (informs ... Management, UX Localization, or Natural Language Processing (NLP) * Minimum of five (5) years ...

Conduct applied research in the field of expertise that contributes to the programs (informs ... Management, UX Localization, or Natural Language Processing (NLP) * Minimum of five (5) years ...

Participate in the defense phase of RFXs * Assist in Lab product evaluation * Develop relationships ... R&D, Support, Program Management. * Comfortable in a Lab setting working with testing equipment ...

Lead and assist with incident response to user-reported issues and operational notifications so as ... Able to effectively prioritize a wide range of responsibilities, managing multiple projects ...

Showing results 21-40

Research Assistant Lab Manager information

What is a research assistant lab manager?

Research Assistant Lab Managers are professionals who oversee the daily operations of research laboratories while also assisting with scientific experiments and projects. Their responsibilities typically include managing lab supplies, maintaining equipment, ensuring safety protocols are followed, and coordinating the work of other lab staff or students. They often assist principal investigators with experiment design, data collection, and analysis. Effective lab managers balance administrative duties with hands-on research support, making them essential for efficient and safe lab environments.

What are the key skills and qualifications needed to thrive as a research assistant lab manager, and why are they important?

To thrive as a Research Assistant Lab Manager, you need a solid background in laboratory techniques, experimental design, and data analysis, typically supported by a relevant bachelor's or master's degree. Familiarity with lab management software, safety protocols, and equipment maintenance is essential, along with certifications such as CITI or GLP if required. Strong organization, attention to detail, leadership, and communication skills help coordinate team efforts and ensure smooth lab operations. These skills are crucial for maintaining research quality, safety, and productivity in a collaborative scientific environment.

What are some common challenges faced by research assistant lab managers, and how can they be addressed?

Research Assistant Lab Managers often encounter challenges such as balancing administrative duties with hands-on research tasks, maintaining strict laboratory safety protocols, and managing inventory or equipment issues. Effective time management and clear communication with both research staff and principal investigators can help address these challenges. Additionally, staying organized and proactively scheduling regular maintenance or safety checks ensures a smoother workflow and helps prevent disruptions in research activities.

What is the difference between Research Assistant Lab Manager vs Research Assistant?

AspectResearch Assistant Lab ManagerResearch Assistant
CredentialsBachelor's or Master's in relevant field; some managerial experienceBachelor's or Master's in relevant field; no managerial experience typically required
Work EnvironmentLaboratory setting, overseeing lab operationsAssisting with experiments and data collection in labs
ResponsibilitiesManaging lab staff, maintaining equipment, ensuring safety protocolsSupporting research activities, data analysis, preparing reports

The Research Assistant Lab Manager role combines research support with lab management duties, requiring leadership skills and organizational abilities. In contrast, the Research Assistant primarily focuses on assisting with experiments and data collection. Both roles are essential in research settings but differ in scope and responsibilities.

What job categories do people searching Research Assistant Lab Manager jobs in Quebec look for?

The top searched job categories for Research Assistant Lab Manager jobs in Quebec are:

What cities in Quebec are hiring for Research Assistant Lab Manager jobs?

Cities in Quebec with the most Research Assistant Lab Manager job openings:

Full-time

Medical, Retirement, PTO

Posted 23 days ago


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 Method Development Research Scientist (Large Molecule) for our Bioanalysis team at the Laval location, you will act as a Study Director responsible for the conduct of all analytical and/or bioanalytical studies using LC-MS/MS, HPLC-UV or any other analytical detection method, in compliance with the Good Laboratory Practice (GLP) Regulations of the Organisation for Economic Co-operation and Development Principles and the US Food and Drug Administration (21 CFR Part 58 and subsequent amendments).

In this role, primary responsibilities include:

  • Developing workflows and assays for the analysis of proteins, peptides, and their post-translational modifications across a variety of biological matrices;
  • Designing and executing laboratory experiments, including sample preparation, mass spectrometry analysis, and data interpretation;
  • Presenting complex datasets in a clear and concise manner to internal teams, clients, and stakeholders;
  • Training Associate Scientists and Analysts on sample preparation procedures and analytical techniques;
  • Preparing, reviewing, and maintaining analytical procedures;
  • Providing scientific recommendations to improve platform performance and data quality;
  • Evaluating and implementing new technologies, tools, and reagents to enhance analytical capabilities and operational efficiency.
Key Elements

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

  • Master degree in Chemistry, Biochemistry or any other related field with at least 2 to 3 years’ experience in a Scientific position;
  • PhD degree in Chemistry, Biochemistry or any other related field;
  • Significant experience using LC-MS/MS and HPLC-UV with chromatographic data system;
  • Very efficient time management;
  • Excellent organizational, interpersonal and communication skills.

 

Role Specific Information:

 

  • Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
  • Transportation: Free parking. Near the Montmorency Subway. 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;
  • 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.


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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