Job Overview As a Research Scientist for our Immunotoxicology team at the Senneville location, you will serve as a Study Scientist or Principal Investigator responsible for the design, conduct and ...
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Research Associate information
See Quebec salary details
$9.86 - $12.74
2% of jobs
$12.74 - $15.63
6% of jobs
$15.63 - $18.51
9% of jobs
$19.82 is the 25th percentile. Wages below this are outliers.
$18.51 - $21.39
17% of jobs
$21.39 - $24.28
15% of jobs
The median wage is $24.38 / hr.
$24.28 - $27.16
16% of jobs
$29.97 is the 75th percentile. Wages above this are outliers.
$27.16 - $30.05
10% of jobs
$30.05 - $32.93
10% of jobs
$32.93 - $35.82
8% of jobs
$35.82 - $38.70
4% of jobs
$38.70 - $41.59
3% of jobs
$9
$26
$41
How much do research associate jobs pay per hour?
What are the key skills and qualifications needed to thrive as a Research Associate, and why are they important?
Is CRA an entry level job?
What are Research Associates?
How much does a research associate earn?
What Does a Research Associate Do?
As a research associate, you conduct research and analysis as directed by a senior researcher or project manager. Researchers work in a number of fields, including medical science, the social sciences, natural sciences, finance, management, and academia. Your specific duties and responsibilities differ depending on the field in which you work, but some features of your work are similar across industries. You typically do primary and secondary source research, organize and process data, analyze said data, and report on your findings to lead researchers or clinicians.
What are some typical challenges a Research Associate might face when managing multiple research projects simultaneously?
What is the difference between Research Associate vs Research Scientist?
| Aspect | Research Associate | Research Scientist |
|---|---|---|
| Required Credentials | Bachelor's or Master's degree in relevant field | Master's or PhD in relevant field |
| Work Environment | Laboratories, research institutions, universities | Laboratories, research institutions, industry settings |
| Employer & Industry Usage | Academic, government, non-profit | Academic, industry, biotech, pharma |
| Common Search & Comparison | Yes | Yes |
The main difference between a Research Associate and a Research Scientist lies in their educational requirements and level of experience. Research Associates typically hold a bachelor's or master's degree and assist in research projects, while Research Scientists usually have a PhD and lead research efforts. Both roles work in similar environments like labs and research institutions, but Research Scientists often have more independence and responsibility.
What is the work of a research associate?
What qualifications do you need to be a research associate?

Full-time
Medical, Retirement, PTO
Re-posted yesterday
Charles River Laboratories rating
8.3
Based on 93 frontline employees who took The Breakroom Quiz
18th of 74 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.
As a Research Scientist for our Immunotoxicology 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.
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 BD flow cytometer platforms; spectral flow cytometry experience is an asset;
- Experience with immunoassay techniques (ELISAs, ECLs, Luminex) and cell-based assays (ELISpot, bioassays) 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.
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
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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