Data Reviewer I

Charles River Laboratories; Laval; On-site; CAD 26,000 - 38,000; Full time

Benefits offered by this job

Annual bonus

3 weeks vacation

5 personal days

Job summary

Charles River Laboratories in Laval, QC, is seeking a Data Reviewer for our Toxicology team. You will review data in accordance with GLP/SOP/IACUC and help maintain data integrity, with a 37.5-hour work week and a $23.25/hour base pay.

Permanent, full-time position with potential overtime or weekends as needed. Benefits, bonus eligibility, and relocation/parking details are provided in the offer package.

Qualifications

• 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.

Responsibilities

• 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 GLP, SOP and IACUC rules.
• Finalize the revision and corrections of the data, according to prescribed deadlines.
• Document deviations in procedures in the DEVIL system in a timely and appropriate manner.
• Collaborate with the various resource persons to maintain high quality in data documentation.

Skills

Attention to details

Observation

Organizational skills

Education

Collegial diploma in Biology, Animal Science or any other related field

Job description

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.

Job Overview

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.

Key Elements

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.

Why Charles River ?

• 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!

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 300 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 20,000 employees within 110 facilities in over 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.

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‑wellness of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

We’re committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

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 [e-mail]. 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.