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Data Reviewer (Immunology and Analytical Chemistry)

Charles River

Sherbrooke

On-site

CAD 60,000 - 80,000

Full time

2 days ago
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Job summary

A global contract research organization in Sherbrooke is looking for a Data Reviewer to ensure that work quality meets regulatory standards. The ideal candidate will have a collegial diploma or B.Sc. in Science, be detail-oriented, and able to work independently. This full-time position offers competitive benefits, including vacation, health coverage, and career development opportunities.

Benefits

3 weeks vacation & Personal days
Health & dental coverage (up to 85% premiums)
Access to savings and retirement program
Free gym on site
Access to telemedicine services

Qualifications

  • Able to work at a computer in a stationary position at least 80% of the time.
  • Reading and writing in English is required.

Responsibilities

  • Ensure the integrity of review and corrections in accordance with GLP and SOP.
  • Finalize revisions and corrections on time.
  • Document any comments outstanding at the end of the review process.

Skills

Detail-oriented
Autonomous
Good observation skills
Bilingualism (English and French)

Education

Collegial diploma in Science or B. Sc. degree in Biology or related field
Job description
Overview

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 Summary

Data Reviewer – Immunology and Analytical Chemistry

As a Data Reviewer for our Immunology and Analytical Chemistry team at the Sherbrooke location, you will you will ensure that the quality of the work is up to the regulatory standards.

In this role, primary responsibilities include :

  • Ensure the integrity of review and corrections in accordance with Good Laboratory Practice (GLP), Standard Operating Procedures (SOP), Analytical Procedures (AP) and study plans.
  • Ensure that all relevant data is reviewed.
  • Be able to finalize revisions and corrections on time, according to predetermined dates.
  • Be proactive in obtaining responses to errors detected. Be responsible for documenting any comments still outstanding at the end of the review process.
Key Elements

If you have the following qualifications, we'll train you for the rest :

  • Collegial diploma in Science or B. Sc. degree in Biology or related field;
  • Be able to work at a computer in a stationary position at least 80% of the time
  • Must be Autonomous
  • Must be detail oriented and have a good observation skills
  • Reading and writting English is required. Bilingualism is preferable.
Role Specific Information
  • Location : 1580 rue Ida-Métivier, Sherbrooke (Fleurimont), QC, J1E 0B5;
  • Transportation : Easily accessible using Sherbrooke’s public transit system. Free parking. Electric vehicle charging station;
  • Salary : 23.00$ / hrs
  • Schedule : Full time, permanent position (37.5 hours / week), depending on the needs, you may have to do overtime. Mostly to work from Monday to Friday.
Why Charles River?
  • 3 weeks’ vacation & Personal days.
  • Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage).
  • Access to a savings and retirement program that includes an employer contribution.
  • 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).
  • Free gym on site.

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

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-being 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.

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