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 ...
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 ...
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 ...
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 ...
Scientist, R&D Proteomics
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
Scientist, R&D Proteomics
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 ...
Research Associate
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 ...
Research Associate
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 ...
Research Associate
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 ...
Research Associate
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 ...
Research Associate
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 ...
Research Associate
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 ...
Research Associate
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 ...
Research Associate
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 ...
Associate Scientist (BSD)
Laval, QC · On-site
About The Role The Associate Scientist is the right-hand help for the senior scientist. As such ... The requirement to have study protocols, designs and clinical research documents written and ...
New
Associate Scientist (BSD)
Laval, QC · On-site
About The Role The Associate Scientist is the right-hand help for the senior scientist. As such ... The requirement to have study protocols, designs and clinical research documents written and ...
New
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 ...
Senior Clinical Research Associate
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 ...
Senior Clinical Research Associate
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 ...
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 ...
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 ...
Clinical Research Associate
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 ...
Clinical Research Associate
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 ...
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 ...
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 ...
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 ...
New
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 ...
New
NSERC Tier 1 Canada Research Chair in electrochemical technologies and functional materials for envi
... 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 ...
NSERC Tier 1 Canada Research Chair in electrochemical technologies and functional materials for envi
... 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 Research Scientist information
What is the difference between Associate Research Scientist vs Research Scientist?
| 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.
What does an Associate Research Scientist do?
What are typical collaboration opportunities for an Associate Research Scientist within a research team?
What are the key skills and qualifications needed to thrive as an Associate Research Scientist, and why are they important?

Other
Medical, Retirement, PTO
Posted 5 days ago
Charles River Laboratories rating
8.3
Based on 93 frontline employees who took The Breakroom Quiz
20th 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.
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.
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.
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