Job Overview As a Method Development Research Scientist (Large Molecule) for our Bioanalysis team ... Training Associate Scientists and Analysts on sample preparation procedures and analytical ...
New
Job Overview As a Method Development Research Scientist (Large Molecule) for our Bioanalysis team ... Training Associate Scientists and Analysts on sample preparation procedures and analytical ...
New
Job Overview As a Method Development Research Scientist (Large Molecule) for our Bioanalysis team ... Training Associate Scientists and Analysts on sample preparation procedures and analytical ...
New
Montreal, QC · On-site
Train Research Associates on sample preparation and analytical techniques * Provide scientific recommendations to improve data quality and platform performance * Monitor data quality and take ...
Quick apply
Montreal, QC · On-site
Train Research Associates on sample preparation and analytical techniques * Provide scientific recommendations to improve data quality and platform performance * Monitor data quality and take ...
CA$35.37/hr
Research Associate - Canada Excellence Research Chair in Metabolism and the Brain (CERC M&B ... Research: Work with scientists, HQPs and students to develop experimental hypotheses, protocols and ...
CA$35.37/hr
Research Associate - Canada Excellence Research Chair in Metabolism and the Brain (CERC M&B ... Research: Work with scientists, HQPs and students to develop experimental hypotheses, protocols and ...
CA$35.37/hr
Research Associate - Canada Excellence Research Chair in Metabolism and the Brain (CERC M&B ... Research: Work with scientists, HQPs and students to develop experimental hypotheses, protocols and ...
CA$35.37/hr
Research Associate - Canada Excellence Research Chair in Metabolism and the Brain (CERC M&B ... Research: Work with scientists, HQPs and students to develop experimental hypotheses, protocols and ...
CA$35.37/hr
The Research Associate will work in collaboration with the Research Supervisor, to develop and ... Qualifications: PhD in computer science required. Experience in linguistics and a strong work ...
CA$35.37/hr
The Research Associate will work in collaboration with the Research Supervisor, to develop and ... Qualifications: PhD in computer science required. Experience in linguistics and a strong work ...
CA$35.37/hr
The Research Associate will work in collaboration with the Research Supervisor, to develop and ... Qualifications: PhD in computer science required. Experience in linguistics and a strong work ...
CA$35.37/hr
The Research Associate will work in collaboration with the Research Supervisor, to develop and ... Qualifications: PhD in computer science required. Experience in linguistics and a strong work ...
Senior Clinical Research Associate - Cardio Device - Canada ICON is a global healthcare ... A bachelor's degree is required, preferably a Bachelor of Science Degree in Life Science, Physical ...
Senior Clinical Research Associate - Cardio Device - Canada ICON is a global healthcare ... A bachelor's degree is required, preferably a Bachelor of Science Degree in Life Science, Physical ...
As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside ... We offer an unparalleled experience, where you can drive remarkable scientific breakthroughs and be ...
As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside ... We offer an unparalleled experience, where you can drive remarkable scientific breakthroughs and be ...
As a Clinical Research Associate (CRA), you will monitor the progress of clinical studies, either ... Bachelor's degree, or its international equivalent in a scientific or health-related field or an ...
As a Clinical Research Associate (CRA), you will monitor the progress of clinical studies, either ... Bachelor's degree, or its international equivalent in a scientific or health-related field or an ...
Montreal, QC · On-site +1
As a Clinical Research Associate (CRA), you will monitor the progress of clinical studies, either ... Bachelor's degree, or its international equivalent in a scientific or health-related field or an ...
Montreal, QC · On-site +1
As a Clinical Research Associate (CRA), you will monitor the progress of clinical studies, either ... Bachelor's degree, or its international equivalent in a scientific or health-related field or an ...
Montreal, QC · On-site
CA$110K - CA$150K/yr
Apply specialized skills and fundamental data science methods such as predictive factor modeling, time series forecast or deep learning, to build new equity returns forecasting models. * Properly ...
Montreal, QC · On-site
CA$110K - CA$150K/yr
Apply specialized skills and fundamental data science methods such as predictive factor modeling, time series forecast or deep learning, to build new equity returns forecasting models. * Properly ...
Bachelor's degree in science from an accredited university; * At least 1 year as a Clinical Research Associate or Clinical Research Coordinator; * Bilingual in English and French; * Thorough ...
Bachelor's degree in science from an accredited university; * At least 1 year as a Clinical Research Associate or Clinical Research Coordinator; * Bilingual in English and French; * Thorough ...
Bachelor's degree in science from an accredited university; * At least 1 year as a Clinical Research Associate or Clinical Research Coordinator; * Bilingual in English and French; * Thorough ...
Bachelor's degree in science from an accredited university; * At least 1 year as a Clinical Research Associate or Clinical Research Coordinator; * Bilingual in English and French; * Thorough ...
Bachelor's degree in science from an accredited university; * At least 1 year as a Clinical Research Associate or Clinical Research Coordinator; * Bilingual in English and French; * Thorough ...
Bachelor's degree in science from an accredited university; * At least 1 year as a Clinical Research Associate or Clinical Research Coordinator; * Bilingual in English and French; * Thorough ...
Montreal, QC · On-site
Bachelor's degree in a scientific or healthcare-related field. * Minimum of 2 years of experience as a Clinical Research Associate. * In-depth knowledge of clinical trial processes, regulations, and ...
Montreal, QC · On-site
Bachelor's degree in a scientific or healthcare-related field. * Minimum of 2 years of experience as a Clinical Research Associate. * In-depth knowledge of clinical trial processes, regulations, and ...
Montreal, QC · On-site
Clinical Research Associate ICON is a global healthcare intelligence and clinical research ... University degree in medicine, science, or equivalent * Knowledge of ICH-GCP guidelines and the ...
Montreal, QC · On-site
Clinical Research Associate ICON is a global healthcare intelligence and clinical research ... University degree in medicine, science, or equivalent * Knowledge of ICH-GCP guidelines and the ...
Trois-rivieres, QC · On-site
... Sciences and Engineering Research Council of Canada (NSERC) Tier 1 Canada Research Chair. More ... The UQTR-INRS Joint Research Unit employs a coordinator, a technician, two research associates ...
Trois-rivieres, QC · On-site
... Sciences and Engineering Research Council of Canada (NSERC) Tier 1 Canada Research Chair. More ... The UQTR-INRS Joint Research Unit employs a coordinator, a technician, two research associates ...
About The Role The Lead Clinical Research Associate (Lead CRA/LCRA) is responsible for overseeing ... Bachelor's degree in a scientific or healthcare-related field preferred * Minimum of 5 years of ...
About The Role The Lead Clinical Research Associate (Lead CRA/LCRA) is responsible for overseeing ... Bachelor's degree in a scientific or healthcare-related field preferred * Minimum of 5 years of ...
... Associate Professor (Clinical). The professorial rank will be determined according to the ... Clinician-Scientists with MD-PhD, or equivalent research-intensive training, are strongly ...
... Associate Professor (Clinical). The professorial rank will be determined according to the ... Clinician-Scientists with MD-PhD, or equivalent research-intensive training, are strongly ...
... Associate Professor (Clinical). The professorial rank will be determined according to the ... Clinician-Scientists with MD-PhD, or equivalent research-intensive training, are strongly ...
... Associate Professor (Clinical). The professorial rank will be determined according to the ... Clinician-Scientists with MD-PhD, or equivalent research-intensive training, are strongly ...
| Aspect | Associate Research Scientist | Research Scientist |
|---|---|---|
| Required Credentials | Bachelor's or Master's degree, some experience | Master's or Ph.D., more extensive research experience |
| Work Environment | Laboratory or research settings, often in academia or industry | Similar environments, often with increased responsibilities |
| Employer & Industry Usage | Research institutions, biotech, pharma, academia | Research institutions, biotech, pharma, academia |
In summary, an Associate Research Scientist typically holds a bachelor's or master's degree and has limited research experience, working under supervision. A Research Scientist usually has a master's or Ph.D. with more independent research responsibilities. Both roles are common in research-focused industries and share similar work environments, but the Research Scientist position generally requires more advanced credentials and experience.

Full-time
Medical, Retirement, PTO
Posted yesterday
New
8.3
Based on 93 frontline employees who took The Breakroom Quiz
19th of 86 rated pharmaceutical
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 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:
We are looking for the following minimum qualifications for this role:
Role Specific Information:
Why Charles River ?
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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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.
Scientific research and development services
10,000+ Employees
Wilmington, MA, US
1947