Data Reviewer - Immunology at Charles River Laboratories
Laval, QC, Canada -
Full Time


Start Date

Immediate

Expiry Date

04 Dec, 25

Salary

23.0

Posted On

06 Sep, 25

Experience

1 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Pharmaceuticals

Description

At Charles River, we are passionate about improving the quality of people’s lives. When you join our global family, you will help create healthier lives for millions of patients and their families.
Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career.
As a Charles River employee, you will be part of an industry-leading, customer-focused company at the forefront of drug development. Your skills will play a key role in bringing life-saving therapies to market faster through simpler, quicker, and more digitalized processes. Whether you are in lab operations, finance, IT, sales, or another area, when you work at Charles River, you will be the difference every day for patients across the globe.

JOB SUMMARY

As a Data Reviewer for our Immunology team at the Laval location, you will verify data for completeness and Good Laboratory Practice (GLP) compliance. You will also promote awareness of best practices related to data collection.

In this role, primary responsibilities include:

  • Perform accurate raw data review and corrections according to GLP regulations, SOPs and study plan requirements;
  • Ensure that the review and corrections are finalized according to established due dates;
  • Answer QA reports promptly and in a clear and concise manner, when required;
  • Comply at all times with all departmental and company Standard Operating Procedures (SOPs) and Study Plans (SPs).

KEY ELEMENTS

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

  • Collegial diploma in Sciences or in related field;
  • A minimum of 1 year of relevant experience working in a Lab environment and GLP experience;
  • Detail oriented and meticulous;
  • Good observation & organizational skills;
  • Ability to work under time constraint and adapt to change.
Responsibilities

ROLE SPECIFIC INFORMATION:

  • Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;

  • Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;

  • Salary: $23/hrs;
  • Annual bonus based on performance;
  • Schedule: Monday to Friday, daytime. Depending on the needs, you may have to do overtime;
  • Permanent position as of the hiring, full-time 37.5hrs per week.

In this role, primary responsibilities include:

  • Perform accurate raw data review and corrections according to GLP regulations, SOPs and study plan requirements;
  • Ensure that the review and corrections are finalized according to established due dates;
  • Answer QA reports promptly and in a clear and concise manner, when required;
  • Comply at all times with all departmental and company Standard Operating Procedures (SOPs) and Study Plans (SPs)

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

  • Collegial diploma in Sciences or in related field;
  • A minimum of 1 year of relevant experience working in a Lab environment and GLP experience;
  • Detail oriented and meticulous;
  • Good observation & organizational skills;
  • Ability to work under time constraint and adapt to change
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