Data Reviewer – Toxicology

Accepting BioReady™: Yes
Category: Clinical Research
Education: Diploma/DEC
Experience: 4-6 Years
Location: Laval, QC
Posted: May 4, 2021
Closes: June 4, 2021

Job description:

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 Summary

We are seeking a Data Reviewer for our Toxicology department site located in Laval (Greater Montreal area) in Canada.

The following are responsibilities related to the Data Reviewer position :

  • Ensure that all calculations related to studies have been verified;
  • Work closely with veterinarians and study directors on certain aspects of the studies;
  • Provide assistance and training in data collection and reporting at all times;
  • Contribute to standardization of procedures;
  • Ensure the study plans and amendments have been read and are understood by all technicians involved in the studies before the start of each study.

The following are minimum qualifications related to the Data Reviewer position:

  • Collegial diploma in animal health care or equivalent;
  • A minimum of 3 years of relevant experience in a GLP environment;
  • Practical knowledge of related legislation, principles, practices and procedures;
  • Strong knowledge and application of GLP;
  • Bilingualism (French and English) is mandatory;
  • Strong problem-solving and analytical skills.

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.

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