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| Job Location | Senneville, QC |
| Education | Not Mentioned |
| Salary | Not Disclosed |
| Industry | Not Mentioned |
| Functional Area | Not Mentioned |
| Job Type | Full Time |
For 70 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.IMPORTANT: In order to be considered for this position, a resume/CV must be uploaded and submitted during the application process. Please make sure work history and education are added correctly.Job SummaryVerification of raw data according to Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Analytical Procedures (AP), and study plans . We are seeking a Coordinator in Data Reviewer for our Biomarkers group located at Senneville, Qc.The following are responsibilities related to the position:Guarantee accurate review and corrections in accordance with Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Analytical Procedures (AP) and study plans.Ensure that all pertinent data is reviewed.Ensure that the review and corrections are finalized according to established due dates.Proactive in obtaining answers to findings. Responsible for documenting any remaining issues at data review clearance.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.Be able to work in team. Have a positive attitude. Adapt to changes.Regularly operates a computer and other office productivity machinery.Must be able to remain in a stationary position at least 80% of the time.IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV.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 120 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.Quick Apply