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Charles River Laboratories, Inc.: Data Reviewer In Genetic Toxicology

Charles River Laboratories, Inc.

This is a Full-time position in Senneville, QC posted October 20, 2020.

Verification of raw data according to Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Analytical Procedures (AP), Study Plans, Protocols and Reports.We are seeking a Data Reviewer for our Genetic Toxicology group located at Senneville, Qc.The following are responsibilities related to the:Guarantee accurate review and corrections in accordance with Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Analytical Procedures (AP), Study Plans, Protocols and Reports.Ensure that all data is reviewed at 100%.Ensure that the review clearance and corrections respect the established due dates.Proactive in obtaining answers to findings.

Perform all other related duties as assigned.The following are minimum qualifications related to the position:DEC in sciences or AECAn equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.Good organizational skillBe able to communicate well with the scientific and technical teams.

Have a positive attitude.

Adapt to changes.A computer knowledge is an asset.Must be able to remain in a stationary position at least 80% of the time.About Safety AssessmentCharles 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 RiverCharles 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 17,000 employees within 90 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.

And in 2019, revenue increased to $2.62 billion.

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 ~85% of the drugs approved by the FDA in 2019.

Equal Employment Opportunity Charles River Laboratories is an Equal Opportunity Employer M/F/Disabled/Vet 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.

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