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Research Scientist
4 months ago
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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 SummaryAs a Research Scientist in Molecular Biology in our immunology team located at the Senneville site, you will be responsible for designing and executing scientific testing strategies and studies.
as well as directing assay development, assay validation, or study conduct; Examine and interpret study data, communicate results to clients and write final reports; Act as project scientist, principal investigator, collaborating scientist, project manager or study director, as applicable; Ensure compliance with protocols and all applicable SOPs; Troubleshoot and resolve analytical or technical problems in the laboratory when scientific expertise is necessary; May introduce new technologies or improvements in existing technologies and Provide consulting functions to clients who design a program or experiment, deal with the interpretation of specific data sets or, where appropriate, answer questions . regulatory authorities.
In this role, responsibilities may include:
- Support non-clinical studies in assessing vector biodistribution/shedding and/or gene expression as part of safety and/or efficacy assessment;
- Development, optimization and use of qPCR, RT-qPCR, ddPCR, DNA/RNA isolation/quantification assays;
- Write scientific documents, review and interpret the results;
- Analyze scientific problems, troubleshoot analytical methods and technical issues;
- Communicates results to clients and advises clients based on knowledge, experience, best practices and regulatory guidance;
- Management of scientific projects and technical resources involved in study conduct.
If you possess the followingqualitifications, we will train you in the rest:
- Possess a M.Sc. or PhD in Immunology, microbiology or virology, or in related scientific discipline, or have relevant experience;
- Is computer literate (Microsoft Word and Excel) and possess excellent communication, interpersonal and teamwork abilities;
- Is fluent in French and English. Bilingualism is preferred;
- Has GLP knowledge (is an asset)
- Competitive benefits upon hire. We pay up to 85% of premiums (medical & dental coverage)
- Employee and family assistance program
- 24/7 access to a doctor and various health care professionals (telemedicine)
- 3 weeks’ Vacation & 10 Personal day policy
- Numerous organized social activities
If you want to contribute to the well-being of our communities, not only across the country, but around the world, join the team, 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 supported the development of 86% of the drugs approved by the FDA in 2021.
Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.
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 [email protected] . 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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