Data Reviewer

For 75 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.

As a Data Reviewer for our Toxicology team at the Laval location, you will be reviewing data while respecting established processes.

In this role, primary responsibilities include:

• Review the data collected on the colonies, for the maintenance of the vivarium spaces, for the management of the equipment or other which is not related to the studies of the customers;
• Ensure the integrity of the studies and meet the regulatory agencies requirements by reviewing data according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP) and the Institutional Animal Care and Use Committee (IACUC) rules;
• Be able to finalize the revision and corrections of the data, according to the prescribed deadlines;
• Document deviations in procedures in the DEVIL system in a timely and appropriate manner;
• Collaborate with the various resource persons in order to maintain a high level of quality in the documentation of the data.

We are looking for the following minimum qualifications for this role:

• Collegial diploma in Biology, Animal Science or any other related field;
• At least 3 years’ experience in a Good Laboratory Practices (GLP) environment;
• Good attention to details;
• Good observation & organizational skills.

Role Specific Information:

• Location:
  
  445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
• Transportation:
  Free parking. Near the Montmorency Subway. Electric vehicle charging station;
• Annual bonus based on performance;
• Schedule:
  
  Monday to Friday daytime. Depending on the needs you may have to do overtime or weekends;
• Permanent position as of the hiring, full-time 37.5hrs per week;
• Salary: $23.25/hr.

• We offer competitive benefits and advantages from day one to support your well-being;
• Employee and family assistance program;
• Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
• Access to a doctor and various health professionals (telemedicine);
• 3 weeks’ Vacation & 5 Personal day policy;
• Many social activities!

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.

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,…