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Data Management Specialist - Analytical Chemistry
Charles River Laboratories International Inc (CRL)
Montreal (Senneville), Quebec, CA, H9X 3R3
Job Summary
As a Data Management Specialist for the Analytical Chemistry Department located at the Sennevile site, you will assist the laboratory scientists in preparing study deliverables, such as analytical result tables and study reports, while meeting deadlines and maintaining quality of work in accordance with Good Laboratory Practices (GLP), Standard Operating Procedures (SOPs), Analytical Procedures (APs) and study plans.
In this role, responsibilities may include
- Contribute to the quality of the study by reviewing the SOPs, procedure forms or other documents related to the assigned studies.
- Coordinate the submission of documentation and data for review and audit.
- Perform or review tabulation of results
- Participate in writing the study report and study plan
Key Elements
The minimum qualifications sought for this position are:
- Holder of a DEC in science (biotechnology, medical laboratory or equivalent) or an AEC
- Motivated, autonomous and meticulous person
- Reading comprehension in English is mandatory. Bilingualism in French and English is preferred
Specific information about the position
Location: Senneville (Shuttle service between Sainte-Anne-de-Bellevue train station and John Abbott College and Senneville site), Free parkingSalary: Starting at $25.72/hr. Possibility to start at a higher level with specific research experience Schedule: Daytime schedule, Monday to Friday,Permanent position upon hiring, full time at 37.5 hours per week
Why Charles River?
- Competitive benefits upon hire. We pay up to 85% of premiums (medical and dental coverage).
- Paid developmental training
- Free on-site gym
- Employee and family assistance program
- 24/7 access to a physician and various health care professionals (telemedicine)
- 3 weeks vacation and 5 personal days
- Numerous organized social activities
If you want to contribute to the well-being of our communities, not only across the country, but also around the world, join the team, IT'S YOUR TIME!
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.
Equal Employment Opportunity
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 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.
Job posted: 2023-04-26
