Data reviewer Anchem- 18 months contract (Sherbrooke)

Accepting BioReady™: Yes
Category: Clinical Research
Education: Diploma/DEC
Location: Sherbrooke, QC
Posted: June 30, 2020
Closes: July 30, 2020

Job description:

Job Summary

We are seeking a data reviewer for our analytical chemistry department located in Sherbrooke.

The following are responsibilities related to the data reviewer position:

  • Guarantee accurate review and corrections in accordance with Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Analytical Procedures (AP) and study plans.
  • Ensure that all pertinent data is reviewed
  • Ensure that the review and corrections are finalized according to established due dates.
  • Proactive in obtaining answers to findings. Responsible for documenting any remaining issues at data review clearance.
  • Perform all other related duties as assigned.

The following are minimum qualifications related to the data reviewer position:

  • Education : DEC in sciences or AEC
  • Experience : N/a

An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.

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.

Apply Now