Charles River Laboratories Data Reviewer Clinical Pathology in Laval, Canada
Data Reviewer Clinical Pathology
Req ID #: 109697
Laval, Quebec, CA, H7V 4B3
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.
Verify data for completeness and Good Laboratory Practice (GLP) compliance. Promote awareness of best practices related to data collection. We are currently looking for a Data REviewer for our Clinla Laboraory team located in Laval, Quebec.
The following are responsibilities related to the position:
Transcribe data from hand-written data records or computer outputs into formats suitable to meet sponsors needs and requirements;
Prepare tables for reporting and participate to the overall preparation of reports, when required;
Ensure accuracy of all raw data, data transcriptions and that SOP/SP requirements are followed;
Answer QA reports promptly and in a clear and concise manner, when required;
Ensure all tasks are performed in accordance with (GLP), where applicable;
Write and revise SOPs, when required;
Manage time effectively;
Remain informed on all legislation and developments related to job through self-education and external training;
Substitute and/or assist department colleagues;
Perform any other reasonable tasks that may be required.
The following are minimum qualifications related to the role:
Collegial diploma in biology or related health sciences;
A minimum of 3 years of relevant experience in a GLP environment;
Strong knowledge of related legislation, principles, practices and procedures;
Strong knowledge and application of GLP;
Good technical writing ability;
Ability to work very accurately;
Meticulous attention to detail;
Bilingualism (French & English) is mandatory;
Strong organizational, interpersonal and communication skills;
Ability to work under time constraint and adapt to change;
Ability to work in a team environment;
Working knowledge of related computer applications.
Work performed in an office environment;
Considerable sensory attention is required on a regular basis;
Concentration to work in front of a computer;
Work on tight deadlines sometimes.
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 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 120 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 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 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.
Charles River Laboratories
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